FDA guidance

510(k) Submissions for Coagulation Instruments

FDA guidance · issued Jun 19, 2003

Key facts

Title 510(k) Submissions for Coagulation Instruments
Issue date Jun 19, 2003
Document on fda.gov wayback.archive-it.org

At a glance

  • None Product codes referenced
  • None Recognized standards referenced

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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

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