GAUZE SPONGE-NON-STERILE SPONGE— 510(k) K831182

Name: FDA 510(k) clearance K831182
Creator: U.S. Food and Drug Administration
Published: 1983-06-08

Substantially Equivalent

Den Med, Inc.

FDA 510(k) clearance K831182 for GAUZE SPONGE-NON-STERILE SPONGE, Substantially Equivalent on 1983-06-08. Applicant: Den Med, Inc.. Device class: Unclassified.

Clearance details

Applicant: Den Med, Inc.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1983-04-11
Decision date: 1983-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K984187 — CROSSTEX NON-WOVEN SPONGES1999-02-18

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K831183 — GAUZE SPONGE STERILE SPONGE1983-06-08

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