TENET MLTI-POSITIONING SURGICAL STIRRUP SYSTEM— 510(k) K963505

Name: FDA 510(k) clearance K963505
Creator: U.S. Food and Drug Administration
Published: 1997-02-14

Substantially Equivalent

Tenet Medical Engineering

FDA 510(k) clearance K963505 for TENET MLTI-POSITIONING SURGICAL STIRRUP SYSTEM, Substantially Equivalent on 1997-02-14. Applicant: Tenet Medical Engineering. Device class: 2.

Clearance details

Applicant: Tenet Medical Engineering
Product code: Code HHP
Device class: Class 2
Regulation: 21 CFR 884.4900
Advisory panel: Obstetrics/Gynecology
Date received: 1996-09-03
Decision date: 1997-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Calgary, CA

Download summary PDF View on FDA.gov ↗

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