ClearanceBrief
510(k) K970704 ยท GBM Catheter, Urethral

PERSONAL CATHETER

ApplicantRochester Medical Corp., Stewartville MN, US
DecisionSubstantially Equivalent, Mar 13, 1997
ReceivedFeb 26, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970704

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.