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" Act. (b) References in this part to regulatory sections of the Code of Federal Regulations are to Chapter I of Title 21, unless otherwise noted. "
Code of Federal Regulations 21 Parts 800 to 1299 Food and Drugs: Revised as ...
autors: Office of the Federal Register, Office of the Federal Register (U.S.) Staff - 2006 - 796 lapas
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Code of Federal Regulations: Containing a Codification of Documents of ...

1990 - 630 lapas
...shall state why the device is substantially equivalent to other devices, as required by § 807.87. (c) To avoid duplicative listings, a gastroenterology-urology...to Chapter I of Title 21, unless otherwise noted. [52 FR 17737, May 11, 1987; 52 FR 22577, June 12, 1987] § 876.3 Effective dates of requirement for...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1999 - 724 lapas
...equivalent to other devices, as required by §807.87. (c) To avoid dupllcative listings, a cardiovascular device that has two or more types of uses (eg, used...to chapter I of title 21, unless otherwise noted. [52 FR 17735, May 11, 1987] 8870.3 Effective dates of requirement for premarket approval. A device...
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Code of Federal Regulations: Containing a Codification of Documents of ...

2001 - 756 lapas
...required by §807.87 of this chapter. (c) To avoid duplicative listings, a general and plastic surgery device that has two or more types of uses (eg, used...diagnostic device and as a therapeutic device) is listed in one subpart only. (d) References in this part to regulatory sections of the Code of Federal Regulations...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1999 - 372 lapas
...13595, Mar. 13, 1995, unless otherwise noted. Subpart A — General Provisions §328.1 Scope. Reference in this part to regulatory sections of the Code of...are to chapter I of title 21 unless otherwise noted. §328.3 Definitions. As used in this part: (a) Alcohol means the substance known as ethanol, ethyl...
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Code of Federal Regulations: 2000-

1999 - 390 lapas
...each condition in this part and each general condition established in §330.1 of this chapter. (b) References in this part to regulatory sections of...Code of Federal Regulations are to chapter I of title 212 unless otherwise noted. § 346.3 Definitions. As used in this part: (a) Analgesic, anesthetic drug....
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Code of Federal Regulations: Containing a Codification of Documents of ...

2001 - 398 lapas
...each of the general conditions established in §330.1 of this chapter. (b) References in this subpart to regulatory sections of the Code of Federal Regulations...are to chapter I of title 21 unless otherwise noted. § 358.103 Definitions. As used in this subpart: (a) Wart remover drug product. A topical agent used...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 1120 lapas
...each condition in this part and each general condition es-tablished in S 330.1 of this chapter. (b) References in this part to regu-latory sections of...Code of Federal Regulations are to chapter I of title 212 unless otherwise noted. §346.3 Definitions. As used in this part: (a) Analgesic, anesthetic drug....
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The Code of Federal Regulations of the United States of America

1992 - 1016 lapas
...and each general condition established in § 330.1 of this chapter. (b) References in this subpart to regulatory sections of the Code of Federal Regulations...are to chapter I of title 21 unless otherwise noted. § 333.303 Definitions. As used in this subpart: (a) Acne. A disease involving the oil glands and hair...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1993 - 702 lapas
...equivalent to other devices, as required by § 807.87. (c) To avoid duplicative listings, an orthopedic device that has two or more types of uses (eg, used both as a diagnostic device and as a surgical device) is listed in one subpart only. (d) References in this part to regulatory sections...
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The Code of Federal Regulations of the United States of America

1996 - 672 lapas
...equivalent to other devices, as required by §807.87. (c) To avoid duplicative listings, an orthopedic device that has two or more types of uses (eg, used both as a diagnostic device and as a surgical device) is listed in one subpart only. (d) References in this part to regulatory sections...
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