TEKNO-MEDICAL OBSTETRICAL FORCEPS— 510(k) K013747

Name: FDA 510(k) clearance K013747
Creator: U.S. Food and Drug Administration
Published: 2002-02-11

Substantially Equivalent

Tekno Medical Optik-Chirurgie GmbH & Co.

FDA 510(k) clearance K013747 for TEKNO-MEDICAL OBSTETRICAL FORCEPS, Substantially Equivalent on 2002-02-11. Applicant: Tekno Medical Optik-Chirurgie GmbH & Co.. Device class: 2.

Clearance details

Applicant: Tekno Medical Optik-Chirurgie GmbH & Co.
Product code: Code HDA
Device class: Class 2
Regulation: 21 CFR 884.4400
Advisory panel: Obstetrics/Gynecology
Date received: 2001-11-13
Decision date: 2002-02-11
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Tuningen, B.W., DE

Download summary PDF View on FDA.gov ↗

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