 | 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... | |
 | 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.... | |
 | 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... | |
 | 1996 - 672 lapas
...equivalent to other devices, as required by §807.87. (c) To avoid duplicative listings, a neurological device that has two or more types of uses (eg, used...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... | |
 | 1998 - 1120 lapas
...condition. (b) This part does not apply to food, medical devices, or drugs for veteri-nary use. (c) References in this part to regu-latory sections of...to chapter I of title 21, unless otherwise noted. {316.2 Purpose. The purpose of this part is to establish standards and procedures for determining eligibility... | |
 | 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... | |
 | 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... | |
 | 1989 - 464 lapas
...early identification of actions that may significantly affect the quality of the human environment. (e) References in this part to regulatory sections of...to Chapter I of Title 21, unless otherwise noted. § 25.5 Policies. (a) All FDA policies and programs will be planned, developed, and implemented so... | |
 | 1994 - 636 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...part to regulatory sections of the Code of Federal Régulations are to Chapter I of Title 21 unless otherwise noted. s 872.3 Effective dates of requirement... | |
 | 1994 - 640 lapas
...and throat device that has two or more types of uses (eg. used both as a diagnostic device and as » therapeutic device) is listed in one subpart only....are to Chapter I of Title 21 unless otherwise noted. §874.9 {874.3 Effective date« of requirement for premarket approval. A device included in this part... | |
| |
... (d) References in this part to regulatory sections of the Code of Federal Regulations are to Chapter I of Title 21 unless otherwise noted. 
