HYDROFERA FEMORAL WICK— 510(k) K974316

Name: FDA 510(k) clearance K974316
Creator: U.S. Food and Drug Administration
Published: 1998-02-13

Substantially Equivalent

Hydrofera, LLC

FDA 510(k) clearance K974316 for HYDROFERA FEMORAL WICK, Substantially Equivalent on 1998-02-13. Applicant: Hydrofera, LLC. Device class: Unclassified.

Clearance details

Applicant: Hydrofera, LLC
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1997-11-17
Decision date: 1998-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Willimantic, CT, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.