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" ... (d) 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: Containing a Codification of Documents of ... - 311. lappuse
1990
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Code of Federal Regulations: Containing a Codification of Documents of ...

2000 - 736 lapas
...substantially equivalent to other devices, as required by §807.87. (c) To avoid duplicative listings, a dental device that has two or more types of uses (eg, used...in one subpart only. (d) References in this part to regnlatory sections of the Code of Federal Regulations are to chapter I of title 21 unless otherwise...
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Code of Federal Regulations: Containing a Codification of Documents of ...

2001 - 756 lapas
...listings, a radiology device that has two or more types of uses (eg, use both as a diagnostic device and a therapeutic device) is listed in one subpart only....the Code of Federal Regulations are to chapter I of this title 21, unless otherwise noted. §892.3 Effective dates of requirement for premarket approval....
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Code of Federal Regulations: Containing a Codification of Documents of ...

1996 - 700 lapas
...devices, as required by §807.87. (c) To avoid duplicative listings, a dental device that has two or mon types of uses (eg, used both as a diagnostic device...in one subpart only. (d) References in this part to regru latory sections of the Code of Federa Regulations are to Chapter I of Title 21 unless otherwise...
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The Code of Federal Regulations of the United States of America

1998 - 1162 lapas
...1359S. 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

1988 - 590 lapas
...listings, a radiology device that has two or more types of uses (eg, use both as a diagnostic device and a therapeutic device) is listed in one subpart only....References in this part to regulatory sections of the Code ol Federal Regulations are to Chapter I ol this Title 21, unless otherwise noted. § 892.3 Effective...
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Code of Federal Regulations: Containing a Codification of Documents of ...

2000 - 440 lapas
...this subpart and each of the general conditions established in §330.1. (b) References in this subpart to regulatory sections of the Code of Federal Regulations...are to chapter I of title 21 unless otherwise noted. §333.103 Definitions. As used in this subpart: First aid antibiotic. An antibiotic-containing drug...
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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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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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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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The Code of Federal Regulations of the United States of America

1991 - 620 lapas
...required by f 807.87. (c) To avoid duplicative listings, a physical medicine device that has two §890.9 or more types of uses (eg, used both as a diagnostic device and as a therapeutic device) is listed only in one subpart. (d) References in this part to regulatory sections of the Code of Federal Regulations...
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