Progressive Electrical Therapeutics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Progressive Electrical Therapeutics - FDA 510(k) Cleared Devices
10
Total
9
Cleared
0
Denied
Progressive Electrical Therapeutics has 9 FDA 510(k) cleared physical medicine devices. Based in Camdenton, US.
Historical record: 9 cleared submissions from 1991 to 1995.
Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Progressive Electrical Therapeutics
10 devices
Cleared
Jun 02, 1995
THE SIGNATURE SERIES, M IV
Neurology
701d
Cleared
Oct 11, 1994
EURO TECH DIAMOND CHIROPRACTIC TABLE
Physical Medicine
57d
Cleared
Sep 29, 1994
EURO TECH STERLING ROLLER TABLE
Physical Medicine
45d
Cleared
Sep 29, 1994
EURO TECH MARQUISE CHIROPRACTIC TABLE
Physical Medicine
45d
Cleared
Sep 29, 1994
EURO TECH PLATINUM CHIROPRACTIC TABLE
Physical Medicine
45d
Cleared
Jul 13, 1994
THE SIGNATURE SERIES, IMC IV
Physical Medicine
377d
Cleared
Jul 12, 1994
THE SIGNATURE SERIES, IC II
Physical Medicine
376d
Cleared
Apr 06, 1994
THE SIGNATURE SERIES, MAGNUM 100
Physical Medicine
174d
Cleared
Feb 23, 1994
THE SIGNATURE SERIES, IC IV
Physical Medicine
237d
Cleared
Nov 13, 1991
BACK MASTER
Physical Medicine
43d