Quickie Designs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Quickie Designs, Inc. - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
Quickie Designs, Inc. has 5 FDA 510(k) cleared medical devices. Based in Fresno, US.
Historical record: 5 cleared submissions from 1990 to 1997. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Quickie Designs, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Quickie Designs, Inc.
6 devices
Cleared
Dec 02, 1997
QUICKIE P90 SERIES
Physical Medicine
172d
Cleared
Apr 28, 1997
QUICKIE P300 SERIES
Physical Medicine
244d
Cleared
Apr 28, 1997
QUICKIE P100 SERIES
Physical Medicine
244d
Cleared
Apr 28, 1997
QUICKIE POWER WHEELCHAIRS P200 SERIES
Physical Medicine
244d
Cleared
Mar 28, 1994
QUICKIE P200
Physical Medicine
580d
Cleared
Feb 15, 1990
QUICKIE P300 WHEELCHAIR
Physical Medicine
23d