Medical Compression Systems (Dbn) , Ltd. is one of 489 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Medical Compression Systems (Dbn) , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ActiveCare Home, ACTIVECARE DVT, ACTIVECARE+SFT, AND ACTIVECARE+DTX SYSTEMS, ACTIVECARE DVT ACTIVECARE+SFT
10
Total
10
Cleared
0
Denied
Medical Compression Systems (Dbn) , Ltd. has 10 FDA 510(k) cleared cardiovascular devices. Based in Ra'Ananna 43373, IL.
Historical record: 10 cleared submissions from 2000 to 2016.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Orly Maor as regulatory consultant.
FDA 510(k) Regulatory Record - Medical Compression Systems (Dbn) , Ltd.
10 devices
Cleared
Jul 13, 2016
ActiveCare Home
Cardiovascular
148d
Cleared
May 08, 2014
ACTIVECARE DVT, ACTIVECARE+SFT, AND ACTIVECARE+DTX SYSTEMS
Cardiovascular
43d
Cleared
Jan 31, 2012
ACTIVECARE DVT ACTIVECARE+SFT
Cardiovascular
63d
Cleared
May 12, 2011
ACTIVECARE SFT
Cardiovascular
113d
Cleared
Mar 08, 2006
ACTIVECARE ++ SYSTEM
Cardiovascular
48d
Cleared
Nov 21, 2002
WIZAIR COMPRESSION SYSTEM
Cardiovascular
28d
Cleared
Mar 27, 2002
WIZAIR DVT
Cardiovascular
202d
Cleared
Aug 25, 2000
WIZAIR COMPRESSION SYSTEM
Cardiovascular
29d
Cleared
May 19, 2000
PROAIR 3000 COMPRESSION SYSTEM
Cardiovascular
196d
Cleared
Mar 03, 2000
SLENDAIR 4000 COMPRESSION SYSTEM
Physical Medicine
94d