FLUFF GAUZE BANDAGE, STERILE & NON-STERILE— 510(k) K953810

Name: FDA 510(k) clearance K953810
Creator: U.S. Food and Drug Administration
Published: 1995-09-14

Substantially Equivalent

K. W. Griffen Co.

FDA 510(k) clearance K953810 for FLUFF GAUZE BANDAGE, STERILE & NON-STERILE, Substantially Equivalent on 1995-09-14. Applicant: K. W. Griffen Co.. Device class: Unclassified.

Clearance details

Applicant: K. W. Griffen Co.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1995-08-08
Decision date: 1995-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, US

Download summary PDF View on FDA.gov ↗

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