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FDA Product Code

FDA Product Code LRZ — Clearance Directory

Device Class
Class I
21 CFR Citation
878.4800

510(k) Clearances — 3 records

K-Number Device Name Applicant Decision Date Clearance Type Summary
K896589 MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERP Optik 1989-12-27 Traditional PDF ↗
K872490 1.1 SCREWDRIVERS Micro-Aire Surgical Instruments, Inc. 1987-07-23 Traditional PDF ↗
K872387 STANDARD SCREW DRIVER Med-Tool, Inc. 1987-07-16 Traditional PDF ↗

Product code LRZ · Class I · General, Plastic Surgery. Data: openFDA.