FDA guidance
User Labeling for Devices that Contain Natural Rubber (21 CFR 801.437); Small Entity…
FDA guidance · Final · issued Apr 1, 2003
Key facts
| Title | User Labeling for Devices that Contain Natural Rubber (21 CFR 801.437); Small Entity Compliance Guide - Guidance for Industry |
|---|---|
| Status | Final |
| Issue date | Apr 1, 2003 |
| Center | Center for Devices and Radiological Health |
| Issuing office | Center for Devices and Radiological Health |
| Communication type | Small Entity Compliance Guide |
| Regulated product | Medical Devices, Radiation-Emitting Products |
| Docket number | FDA-2020-D-0957 |
| Open for comment | No |
| Document on fda.gov | fda.gov |
At a glance
- 1–9 Product codes referenced
- 1–9 Recognized standards referenced
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA guidance documents
FDA guidance documents describe the agency's current thinking on regulatory topics. Drafts are issued for comment before a final version is published.
Source: U.S. Food and Drug Administration (FDA), Guidance Documents