FDA guidance
Guidance on 510(k) Submissions for Implanted Infusion Ports
FDA guidance · issued Oct 1, 1990
Key facts
| Title | Guidance on 510(k) Submissions for Implanted Infusion Ports |
|---|---|
| Issue date | Oct 1, 1990 |
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