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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. "
The Code of Federal Regulations of the United States of America - 356. lappuse
2006
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Code of Federal Regulations: Containing a Codification of Documents of ...

1990
...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
...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
...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
...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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The Code of Federal Regulations of the United States of America

2005
...device that has two or more types of uses (eg, used both as a diagnostic device and as a microbiology device) is listed only in one subpart. (d) References...part to regulatory sections of the Code of Federal §866.9 Regulations are to chapter I of title 21, unless otherwise noted. (e) Guidance documents referenced...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1999
...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
...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
...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
...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 ..., 21. izdevums,800-1299. daļas

1993
...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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