ClearanceBrief
510(k) K922339 ยท MCZ Suture Removal Kit

SUTURE REMOVAL KIT

ApplicantTransidyne General Corp., Spartanburg SC, US
DecisionUnknown, Dec 11, 1992
ReceivedMay 19, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922339

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.