Progress Mankind Technology - FDA 510(k) Cleared Devices
17
Total
16
Cleared
0
Denied
Progress Mankind Technology has 16 FDA 510(k) cleared medical devices. Based in Hopkins, US.
Historical record: 16 cleared submissions from 1980 to 1988. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Progress Mankind Technology Filter by specialty or product code using the sidebar.
17 devices
Cleared
Oct 28, 1988
PMT 3721-1 EPIDURAL KIT
Anesthesiology
85d
Cleared
Sep 09, 1988
PMT MANKIND LUMBAR-PERITONEAL SHUNT MODEL 1115-1
Neurology
150d
Cleared
Jun 19, 1987
PMT TRACTION TONGS
Neurology
52d
Cleared
Feb 13, 1986
PMT ACCUPRESSURE INFUSION SYSTEM 3601
General Hospital
125d
Cleared
Jul 30, 1985
ELECTRODE FOR NEUROLOGICAL SURGERY 2111
Neurology
215d
Cleared
Jun 26, 1985
TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600
General & Plastic Surgery
181d
Cleared
Feb 17, 1984
PMT-HALO/ORTHOPEDIC JACKET SYSTEM
Neurology
86d
Cleared
Jun 15, 1983
PMT VAXIOM STEREOTACTIC SYS #FX001
Neurology
51d
Cleared
Apr 06, 1983
TEMP TRACE
General Hospital
47d
Cleared
Dec 03, 1981
LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER
Neurology
65d
Cleared
Apr 02, 1981
MODEL 1301 BIOTAC (TM)
General & Plastic Surgery
24d
Cleared
Nov 19, 1980
PMT DEPTHALON DEPTH CORTICOGRAPHY ELEC
Neurology
72d
Cleared
Nov 19, 1980
PMT DEPTHALON DEPTH #2102
Neurology
72d
Cleared
Nov 19, 1980
MICROLET FAMILY OF NEEDLE/DEPTH ELECT-
Neurology
64d
Cleared
Nov 12, 1980
VAXIOM FAMILY OF RF LESION PROBES & ELEC
Neurology
57d
Cleared
May 30, 1980
MACROVAC
General Hospital
18d
Cleared
May 30, 1980
MICROVAC
General Hospital
18d