DYNAREX GAUZE SPONGE OR PADS— 510(k) K933308

Name: FDA 510(k) clearance K933308
Creator: U.S. Food and Drug Administration
Published: 1993-12-22

Substantially Equivalent

Dynarex Corp.

FDA 510(k) clearance K933308 for DYNAREX GAUZE SPONGE OR PADS, Substantially Equivalent on 1993-12-22. Applicant: Dynarex Corp.. Device class: Unclassified.

Clearance details

Applicant: Dynarex Corp.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1993-07-07
Decision date: 1993-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brewster, NY, US

Download summary PDF View on FDA.gov ↗

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K984187 — CROSSTEX NON-WOVEN SPONGES1999-02-18

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