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FDA Product Code

FDA Product Code KDG — Clearance Directory

Device Class
Class I
21 CFR Citation
878.4820

510(k) Clearances — 11 records

K-Number Device Name Applicant Decision Date Clearance Type Summary
K952678 STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT Avail-Southwest Division 1995-07-10 Traditional PDF ↗
K952200 OMNI-JUG Waterstone Medical, Inc. 1995-06-29 Traditional PDF ↗
K894785 SURGICAL CHISEL/OSTEOTOME Fdt Precision Machine Co., Inc. 1989-08-18 Traditional PDF ↗
K891471 SIL-MED WASTE FLUID DUMP BAG Sil-Med Corp. 1989-08-15 Traditional PDF ↗
K872947 POREX QUALITY PLASTIC SURGERY INSTRUMENTS Porex Medical 1987-08-21 Traditional PDF ↗
K872092 OSTEOTOME SET, HOKE, STRAIGHT, SET OF 5 Military Engineering, Inc. 1987-06-23 Traditional PDF ↗
K842824 CHERMEL BONE CHISELS Cher Mel Corp. 1984-08-02 Traditional PDF ↗
K772376 NEIVERT OSTEOTOME Edward Weck, Inc. 1978-03-09 Traditional PDF ↗
K772373 ANDERSON-NEIVERT OSTEOTOME Edward Weck, Inc. 1978-03-09 Traditional PDF ↗
K772374 SILVER OSTEOTOME Edward Weck, Inc. 1978-03-09 Traditional PDF ↗
K780135 CEMENT EXTRACTION INSTRUMENT SET Orthopedic Equipment Co., Inc. 1978-01-31 Traditional PDF ↗

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