ClearanceBrief
510(k) K884198 ยท DQX Wire, Guide, Catheter

TARGET THERAPEUTICS SEEKER-16 STEERABLE GUIDEWIRE

ApplicantTarget Therapeutics, Santa Monica CA, US
DecisionSubstantially Equivalent, Dec 13, 1988
ReceivedOct 6, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884198

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.