Pegasus Airwave, Inc. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Pegasus Airwave, Inc. - FDA 510(k) Cleared Devices
4
Total
3
Cleared
0
Denied
Pegasus Airwave, Inc. has 3 FDA 510(k) cleared medical devices. Based in Hants Po35qt, England, GB.
Historical record: 3 cleared submissions from 1988 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pegasus Airwave, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pegasus Airwave, Inc.
4 devices
Cleared
Mar 17, 1995
PEGASUS BIWAVE PLUS SYSTEM
General Hospital
196d
Cleared
Mar 31, 1994
PEGASUS PROACTIVE WHEELCHAIR CUSHION
Physical Medicine
412d
Cleared
Mar 07, 1994
PEGASUS BIWAVE SYSTEM
General Hospital
259d
Cleared
Feb 22, 1988
PEGASUS AIRWAVE SYST/SPEC MATTRESS DECUBITUS ULCER
General Hospital
101d