VAGINAL RETRACTORS - KRISTELLER, DELEE, BREISKY— 510(k) K891038

Name: FDA 510(k) clearance K891038
Creator: U.S. Food and Drug Administration
Published: 1989-03-17

Substantially Equivalent

Zinnanti Surgical Instruments, Inc.

FDA 510(k) clearance K891038 for VAGINAL RETRACTORS - KRISTELLER, DELEE, BREISKY, Substantially Equivalent on 1989-03-17. Applicant: Zinnanti Surgical Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Zinnanti Surgical Instruments, Inc.
Product code: Code HDL
Device class: Class 1
Regulation: 21 CFR 884.4520
Advisory panel: Obstetrics/Gynecology
Date received: 1989-02-28
Decision date: 1989-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chatsworth, CA, US

Download summary PDF View on FDA.gov ↗

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