ClearanceBrief
510(k) K940208 ยท GFD Dermatome

AESCULAP ACCU-DERMATOME

ApplicantAesculap, Inc., South San Francisco CA, US
DecisionSubstantially Equivalent, Feb 24, 1994
ReceivedJan 14, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940208

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.