ClearanceBrief
Company ยท IL

Medical Compression Systems (Dbn) , Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2016. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
JOWSleeve, Limb, Compressible9
IRPMassager, Powered Inflatable Tube1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 13, 2016K160431ActiveCare Home
Medical Compression Systems (Dbn) , Ltd., IL
JOW
May 8, 2014K140755ACTIVECARE DVT, ACTIVECARE+SFT, AND ACTIVECARE+DTX SYSTEMS
Medical Compression Systems (Dbn) , Ltd., IL
JOW
Jan 31, 2012K113525ACTIVECARE DVT ACTIVECARE+SFT
Medical Compression Systems (Dbn) , Ltd., IL
JOW
May 12, 2011K110159ACTIVECARE SFT
Medical Compression Systems (Dbn) , Ltd., IL
JOW
Mar 8, 2006K060146ACTIVECARE ++ SYSTEM
Medical Compression Systems (Dbn) , Ltd., IL
JOW
Nov 21, 2002K023573WIZAIR COMPRESSION SYSTEM
Medical Compression Systems (Dbn) , Ltd., IL
JOW
Mar 27, 2002K012994WIZAIR DVT
Medical Compression Systems (Dbn) , Ltd., IL
JOW
Aug 25, 2000K002287WIZAIR COMPRESSION SYSTEM
Medical Compression Systems (Dbn) , Ltd., IL
JOW
May 19, 2000K993758PROAIR 3000 COMPRESSION SYSTEM
Medical Compression Systems (Dbn) , Ltd., IL
JOW
Mar 3, 2000K994057SLENDAIR 4000 COMPRESSION SYSTEM
Medical Compression Systems (Dbn) , Ltd., IL
IRP

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes