BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005— 510(k) K954278

Name: FDA 510(k) clearance K954278
Creator: U.S. Food and Drug Administration
Published: 1995-10-02

Substantially Equivalent

Beta Medical Products, Inc.

FDA 510(k) clearance K954278 for BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005, Substantially Equivalent on 1995-10-02. Applicant: Beta Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Beta Medical Products, Inc.
Product code: Code MMZ
Device class: Class 2
Regulation: 21 CFR 876.4890
Advisory panel: Gastroenterology, Urology
Date received: 1995-09-13
Decision date: 1995-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Akron, OH, US

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