ClearanceBrief
510(k) K901767 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

MODIFIED IVT PERIPHERAL ATHERECTOMY

ApplicantIntensive Technology, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Jun 28, 1990
ReceivedApr 17, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901767

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.