M.P. Video, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
M.P. Video, Inc. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1982 to 1995.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by M.P. Video, Inc.
11 devices
Cleared
Jun 30, 1995
COMBINATION CAMERA/LIGHT SOURCE
General & Plastic Surgery
95d
Cleared
Oct 17, 1994
MEDICAM XENON LIGHT SOURCE
General & Plastic Surgery
97d
Cleared
Aug 08, 1994
AUTOCLAVEABLE MEDICAM 900 DIGICON CAMERA
General & Plastic Surgery
83d
Cleared
Jul 18, 1994
MEDICAM 900 REMOTE
General & Plastic Surgery
98d
Cleared
Jun 27, 1994
MEDICAM ENDOCOUPLER AND BEAMSPLITTER
General & Plastic Surgery
82d
Cleared
Jul 24, 1989
ML-800 AUTOELECTRONIC LIGHT SOURCE
General & Plastic Surgery
61d
Cleared
Jul 26, 1988
MEDICAM MC-7 AND RP-7 SURGICAL CAMERAS
General & Plastic Surgery
13d
Cleared
May 07, 1987
SURGICAL CAMERA ACCESSORIES
General & Plastic Surgery
13d
Cleared
Apr 03, 1987
MC-SERIES SURGICAL CAMERAS
General & Plastic Surgery
17d
Cleared
Mar 31, 1987
MEDICAM S-4 SURGICAL CAMERA
General & Plastic Surgery
14d
Cleared
May 03, 1982
MEDICAM
General & Plastic Surgery
39d