ClearanceBrief
510(k) K813103 ยท KDD Kit, Surgical Instrument, Disposable

ACKRAD INCISION & DRAIN SET

ApplicantAckrad Laboratories, Mchenry IL, US
DecisionSubstantially Equivalent, Dec 9, 1981
ReceivedNov 3, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813103

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.