Medical Products Development, Inc. - FDA 510(k) Cleared Devices
13
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medical Products Development, Inc. General & Plastic Surgery ✕
8 devices
Cleared
Feb 26, 1981
SURG-FLEX 10 LIGHT
General & Plastic Surgery
84d
Cleared
Feb 12, 1981
REPLACABLE BATTERY HI-TEMP CAUTERY
General & Plastic Surgery
38d
Cleared
Feb 12, 1981
MULTIHI-TEMP CAUTERY
General & Plastic Surgery
38d
Cleared
Feb 04, 1981
HITEMP. TM 2 LOOPTIP CAUTERY
General & Plastic Surgery
77d
Cleared
Jan 23, 1981
SURG-FLEX 5 SURGICAL LIGHT
General & Plastic Surgery
18d
Cleared
Jan 23, 1981
SURG-FLEX 15 SURGICAL LIGHT
General & Plastic Surgery
18d
Cleared
Nov 12, 1980
HI-TEMP LOOPTIP SURGICAL CAUTERY
General & Plastic Surgery
50d
Cleared
Jun 26, 1980
HI-TEMP SURGICAL CAUTERY
General & Plastic Surgery
20d