ClearanceBrief
510(k) K974393 ยท JOW Sleeve, Limb, Compressible

VASO PRESS SYSTEM

ApplicantBritt Corp., Inc., Freehold NJ, US
DecisionSubstantially Equivalent, Mar 19, 1999
ReceivedNov 21, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K974393

DateFirm and productCodeLinked 510(k)
Apr 8, 2019Compass Health Brands (Corporate Office)
MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S
Terminated
JOWNone listed
Apr 8, 2019Compass Health Brands (Corporate Office)
MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient, Model #6103M-S
Terminated
JOWNone listed
Apr 8, 2019Compass Health Brands (Corporate Office)
MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient, Model #6104M-S
Terminated
JOWNone listed
Apr 8, 2019Compass Health Brands (Corporate Office)
MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient, Model #6103L-S
Terminated
JOWNone listed
Apr 8, 2019Compass Health Brands (Corporate Office)
MediPress pneumatic compression system Full Leg (Short)-Segmental Gradient, Model #6103S-S
Terminated
JOWNone listed
Apr 8, 2019Compass Health Brands (Corporate Office)
MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient, Model #6104S-S
Terminated
JOWNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.