Pdg Product Design Group, Inc. is one of 623 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Pdg Product Design Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Stellar LEAP, ELEVATION, FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50
8
Total
8
Cleared
0
Denied
Pdg Product Design Group, Inc. has 8 FDA 510(k) cleared medical devices. Based in Vancouver, Bc, CA.
Historical record: 8 cleared submissions from 1996 to 2017. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Pdg Product Design Group, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Canopy Medical, LLC.
FDA 510(k) Regulatory Record - Pdg Product Design Group, Inc.
8 devices
Cleared
Jun 27, 2017
Stellar LEAP
Physical Medicine
202d
Cleared
Oct 16, 2014
ELEVATION
Physical Medicine
283d
Cleared
Jan 17, 2007
FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50
Physical Medicine
30d
Cleared
Jun 14, 2006
ASTROTILT MANUAL WHEELCHAIR
Physical Medicine
15d
Cleared
Mar 22, 1999
THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR
Physical Medicine
28d
Cleared
May 09, 1997
ECLIPSE 400 MANUALLY OPERATED WHEELCAIR
Physical Medicine
25d
Cleared
Feb 14, 1997
BENTLEY MANUALLY OPERATED WHEELCHAIR
Physical Medicine
18d
Cleared
May 29, 1996
ECLIPSE 600 MANUALLY OPERATED WHEELCHAIR
Physical Medicine
26d