Progressive Dynamics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Progressive Dynamics, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Progressive Dynamics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Marshall, US.
Historical record: 7 cleared submissions from 1992 to 1996. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Progressive Dynamics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Progressive Dynamics, Inc.
7 devices
Cleared
Jan 17, 1996
LIFE-AIR 1000 HYPOTHERMIC THERAPY SYSTEM
Cardiovascular
244d
Cleared
Nov 01, 1994
LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATOR
Gastroenterology & Urology
40d
Cleared
Nov 09, 1993
LIFE-AIR 1000 PATIENT WARMING COVER
Cardiovascular
110d
Cleared
Oct 28, 1993
LUMINOUS 150 FIBEROPTIC ILLUMINATOR
General & Plastic Surgery
94d
Cleared
Jul 08, 1992
LUMINOUS 250 FIBEROPTIC ILLUMINATOR
General & Plastic Surgery
79d
Cleared
Apr 21, 1992
LIFE-AIR 1000 HYPOTHERMIC TREATMENT SYSTEM
Cardiovascular
203d
Cleared
Mar 30, 1992
LIFE-AIR 1000 PATIENT WARMING COVERS
Cardiovascular
181d