Escada International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Escada International, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Escada International, Inc. has 4 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 4 cleared submissions from 2005 to 2008. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Escada International, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Escada International, Inc.
4 devices
Cleared
Aug 20, 2008
TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM
Physical Medicine
219d
Cleared
Oct 29, 2007
TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS
Physical Medicine
158d
Cleared
Oct 06, 2006
TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS
Physical Medicine
119d
Cleared
Jul 25, 2005
TERRAQUANT MQ2000 LASER THERAPY DEVICE
Physical Medicine
262d