ClearanceBrief
510(k) K012199 ยท GAB Needle, Suturing, Disposable

DIGICAP

ApplicantHumana USA, Inc., Bethesda MD, US
DecisionSubstantially Equivalent, Dec 19, 2001
ReceivedJul 13, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K012199

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.