Progressive Medical Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Progressive Medical Technology, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Progressive Medical Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in Lansing, US.
Historical record: 5 cleared submissions from 1992 to 1993. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Progressive Medical Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Progressive Medical Technology, Inc.
5 devices
Cleared
Mar 22, 1993
OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED
Physical Medicine
238d
Cleared
Feb 11, 1992
TALLEY TM300 SEQUENTIAL MULTICOM COMPRESSION SYST
Physical Medicine
82d
Cleared
Feb 11, 1992
TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST.
Physical Medicine
56d
Cleared
Feb 11, 1992
TALLEY TM200 INTERMTTENT COMPRESSION UNIT
Physical Medicine
56d
Cleared
Jan 13, 1992
B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT
Physical Medicine
49d