LITHOTRITE— 510(k) K760273

Name: FDA 510(k) clearance K760273
Creator: U.S. Food and Drug Administration
Published: 1976-12-06

Substantially Equivalent

V. Mueller O.V. Baxter Healthcare Corp.

FDA 510(k) clearance K760273 for LITHOTRITE, Substantially Equivalent on 1976-12-06. Applicant: V. Mueller O.V. Baxter Healthcare Corp.. Device class: 2.

Clearance details

Applicant: V. Mueller O.V. Baxter Healthcare Corp.
Product code: Code FGK
Device class: Class 2
Regulation: 21 CFR 876.4500
Advisory panel: Gastroenterology, Urology
Date received: 1976-07-22
Decision date: 1976-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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