SHEATH, RESECTOSCOPE— 510(k) K760182

Name: FDA 510(k) clearance K760182
Creator: U.S. Food and Drug Administration
Published: 1976-12-02

Substantially Equivalent

V. Mueller O.V. Baxter Healthcare Corp.

FDA 510(k) clearance K760182 for SHEATH, RESECTOSCOPE, Substantially Equivalent on 1976-12-02. Applicant: V. Mueller O.V. Baxter Healthcare Corp.. Device class: 2.

Clearance details

Applicant: V. Mueller O.V. Baxter Healthcare Corp.
Product code: Code FDC
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1976-07-06
Decision date: 1976-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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