STI TISSUE MANIPULATOR— 510(k) K911699

Name: FDA 510(k) clearance K911699
Creator: U.S. Food and Drug Administration
Published: 1991-06-13

Substantially Equivalent

Surgical Technologies, Inc.

FDA 510(k) clearance K911699 for STI TISSUE MANIPULATOR, Substantially Equivalent on 1991-06-13. Applicant: Surgical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Surgical Technologies, Inc.
Product code: Code HIN
Device class: Class 2
Regulation: 21 CFR 884.4150
Advisory panel: Obstetrics/Gynecology
Date received: 1991-04-16
Decision date: 1991-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chesterfield, MO, US

Download summary PDF View on FDA.gov ↗

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