RUDD-CLINIC HEMORRHOIDAL FORCEPS— 510(k) K800441

Name: FDA 510(k) clearance K800441
Creator: U.S. Food and Drug Administration
Published: 1980-04-08

Substantially Equivalent

J. Sklar Mfg. Co., Inc.

FDA 510(k) clearance K800441 for RUDD-CLINIC HEMORRHOIDAL FORCEPS, Substantially Equivalent on 1980-04-08. Applicant: J. Sklar Mfg. Co., Inc.. Device class: 1.

Clearance details

Applicant: J. Sklar Mfg. Co., Inc.
Product code: Code KOA
Device class: Class 1
Regulation: 21 CFR 876.4730
Advisory panel: Gastroenterology, Urology
Date received: 1980-02-28
Decision date: 1980-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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