R. A. Fischer Co. Corp. - FDA 510(k) Cleared Devices
13
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - R. A. Fischer Co. Corp. General & Plastic Surgery ✕
9 devices
Cleared
Jan 05, 1996
COMPU-BLEND EPILATOR
General & Plastic Surgery
130d
Cleared
Jun 05, 1989
MODEL SE-5 EPILATOR
General & Plastic Surgery
35d
Cleared
Oct 04, 1988
MODEL CBX EPILATOR
General & Plastic Surgery
7d
Cleared
Apr 28, 1987
CB-7 ELECTRONIC EPILATOR
General & Plastic Surgery
21d
Cleared
Nov 08, 1985
ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9
General & Plastic Surgery
147d
Cleared
Sep 26, 1984
ELECTRONIC EPILATOR TS-1
General & Plastic Surgery
51d
Cleared
Jan 14, 1983
HIGH FREQUENCY EPILATOR CB-2
General & Plastic Surgery
38d
Cleared
Jul 28, 1980
EPILATOR, MODEL CP-16
General & Plastic Surgery
49d
Cleared
Jan 24, 1978
EPILATOR, ELECTRONIC MODEL SE-2
General & Plastic Surgery
8d