ClearanceBrief
510(k) K945430 ยท MDM Instrument, Manual, Surgical, General Use

DERMAVBLADE(TM)

ApplicantHasting'S Biomedical Corp., Quincy IL, US
DecisionSubstantially Equivalent, Nov 28, 1994
ReceivedAug 23, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945430

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.