GAUZE CONVERSION CLASS II STERILE— 510(k) K832213

Name: FDA 510(k) clearance K832213
Creator: U.S. Food and Drug Administration
Published: 1983-07-26

Substantially Equivalent

Winn Hirsch & Assoc.

FDA 510(k) clearance K832213 for GAUZE CONVERSION CLASS II STERILE, Substantially Equivalent on 1983-07-26. Applicant: Winn Hirsch & Assoc.. Device class: Unclassified.

Clearance details

Applicant: Winn Hirsch & Assoc.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1983-07-12
Decision date: 1983-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K990974 — VITOP DRESSING1999-06-09
K990584 — GAUZE SPONGES: LAPAROTOMY SPONGE, X-RAY DETECTABLE1999-04-23
K984187 — CROSSTEX NON-WOVEN SPONGES1999-02-18

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K864375 — TYPE 316L COTTER WIRE1987-05-20
K832214 — GAUZE CONVERSION CLASS I-NON-STERILE1983-07-26
K830511 — ZANLEX, ZAN-TEX & ZANDEX1983-03-17
K812390 — NEUROSPONGE PADDIE1981-11-24

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