Briox Technologies, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Briox Technologies, Inc. General & Plastic Surgery ✕
4 devices
Cleared
Jul 24, 1979
BRIOX MODEL 2000-CQ QUIET COMPRESSOR
General & Plastic Surgery
18d
Cleared
Jul 24, 1979
BRIOX MODEL 2000-A ASPIRATOR UNIT
General & Plastic Surgery
18d
Cleared
Jul 24, 1979
BRIOX MODEL 2000-C COMPRESSOR UNIT
General & Plastic Surgery
18d
Cleared
Jul 24, 1979
BRIOX MODEL 2000-CA COMPRESSOR UNIT
General & Plastic Surgery
18d