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FDA Product Code

FDA Product Code GBJ — Clearance Directory

Device Class
Class I
21 CFR Citation
878.3750

510(k) Clearances — 4 records

K-Number Device Name Applicant Decision Date Clearance Type Summary
K934970 DUET Trulife , Ltd. 1993-12-10 Traditional PDF ↗
K810282 OPERATING TABLE ACCESSORY CLAMP Minnesota Scientific, Inc. 1981-02-26 Traditional PDF ↗
K790946 GORDON IVS INTRAVENOUS STABILIZER Whitman Medical Corp. 1979-06-05 Traditional PDF ↗
K790186 PROTECTIVSTABILIZER Jelco Laboratories 1979-02-26 Traditional PDF ↗

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