ClearanceBrief
510(k) K070225 ยท DSP System, Balloon, Intra-Aortic And Control

SUPRACOR INTR-AORTIC BALLOON PUMP CONSOLE

ApplicantAbiomed, Inc., Danvers MA, US
DecisionSubstantially Equivalent, Dec 13, 2007
ReceivedJan 24, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070225

No recall in the FDA data names this 510(k).

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