FDA guidance

Guidance on Premarket Notification [510(K)] Submissions for Short-Term and Long-Term…

FDA guidance · issued Mar 15, 1995

Key facts

Title Guidance on Premarket Notification [510(K)] Submissions for Short-Term and Long-Term Intravascular Catheters
Issue date Mar 15, 1995

At a glance

  • 10–99 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

Browse all FDA guidance documents