 | 2000 - 736 lapas
...equivalent to other devices, as required by §807.87. (c) To avoid duplicative listings, a physical medicine device that has two or more types of uses «eg, used...in this part to regulatory sections of the Code of Fédérai Regulations are to chapter I of title 21. unless otherwise noted. [52 PR 17741, May 11, 1987]... | |
 | 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...regulatory sections of the Code of Federal Regulations are the Chapter I of Title 21, unless otherwise noted. [52 PR 17741, May 11, 1987] §890.3 Effective dates... | |
 | 1988 - 590 lapas
...and personal use device that has two or more types of uses (eg, used both as a diagnostic § 880.2400 device and as a therapeutic device) is listed only...to Chapter I of Title 21, unless otherwise noted. [52 FR 17738, May 11, 1987] § 880.3 Effective dates of requirement for premarket approval. A device... | |
 | 1992 - 626 lapas
...equivalent to other devices, as required by § 807.87. (c) To avoid duplicative listings, a cardiovascular device that has two or more types of uses (eg, used...and as a therapeutic device) is listed only in one sub parted) References in this part to regulatory sections of the Code of Federal Regulations are to... | |
 | 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... | |
 | 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... | |
 | 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... | |
 | 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... | |
 | 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.... | |
 | 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... | |
| |
... (d) References in this part to regulatory sections of the Code of Federal Regulations are to chapter I of title 21. unless otherwise noted. 
