ClearanceBrief
510(k) K953298 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

MS CLASSIQUE BALLOON DIATATION CATHETER

ApplicantMeadox Medicals, Div. Boston Scientific Corp., Oakland NJ, US
DecisionSubstantially Equivalent, Feb 8, 1996
ReceivedJul 14, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953298

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.