STERILE WET DRESSING PACK— 510(k) K781322

Name: FDA 510(k) clearance K781322
Creator: U.S. Food and Drug Administration
Published: 1978-08-17

Substantially Equivalent

W.G. Whitney Corp.

FDA 510(k) clearance K781322 for STERILE WET DRESSING PACK, Substantially Equivalent on 1978-08-17. Applicant: W.G. Whitney Corp.. Device class: Unclassified.

Clearance details

Applicant: W.G. Whitney Corp.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1978-07-31
Decision date: 1978-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EFQ

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K991757 — NON-ABSORBABLE GAUZE FOR EXTERNAL USE, STERILE AND NON STERILE1999-08-12
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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

More clearances from W.G. Whitney Corp.

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K834532 — STERILE WET DRESSING PACK1984-01-25
K813535 — XEROFORM DRESSING1982-02-04
K810406 — STERILE WET DRESSING PACK1981-03-11
K803299 — COLD/HOT PACK1981-01-15
K800907 — TOMAC WET DRESSING WARMER1980-05-20

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