MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERP— 510(k) K896589

Name: FDA 510(k) clearance K896589
Creator: U.S. Food and Drug Administration
Published: 1989-12-27

Substantially Equivalent

Optik

FDA 510(k) clearance K896589 for MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERP, Substantially Equivalent on 1989-12-27. Applicant: Optik. Device class: 1.

Clearance details

Applicant: Optik
Product code: Code LRZ
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1989-11-21
Decision date: 1989-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Criftib, MD, US

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Recent devices under product code LRZ

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K872490 — 1.1 SCREWDRIVERS1987-07-23
K872387 — STANDARD SCREW DRIVER1987-07-16

More clearances from Optik

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K933776 — OPTIK LAPAROSCOPE1994-03-16
K926166 — COAST VIDEO ENDOSCOPIC IMAGING SYSTEM1993-06-01
K896404 — TITAMED ANTWERP SYSTEM1990-04-16
K894557 — LIGHTSCOPE SET1989-08-07
K894558 — MINI LIGHTSCOPE SET, LIGHTSCOPE JR. SET1989-08-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.