Cavitron Corp. - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cavitron Corp. General & Plastic Surgery ✕
4 devices
Cleared
Feb 13, 1981
MINOR SURGERY LIGHT
General & Plastic Surgery
18d
Cleared
Nov 18, 1980
CAVITRON ULTRASONIC SURG. ASPIR. CUSA
General & Plastic Surgery
126d
Cleared
Mar 27, 1978
DIGAPHOT PHOTOTHERAPY METER MODEL PT 145
General & Plastic Surgery
55d
Cleared
Jun 24, 1977
CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5
General & Plastic Surgery
24d