ClearanceBrief
510(k) K780998 ยท GDX Scalpel, One-Piece

SCALPEL

ApplicantIsolab, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 27, 1978
ReceivedJun 14, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780998

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.