ClearanceBrief
510(k) K943603 ยท HET Laparoscope, Gynecologic (And Accessories)

AESCULAP LAPAROSCOPIC ANCILLARY DEVICES

ApplicantAesculap, Inc., South San Francisco CA, US
DecisionSubstantially Equivalent, Mar 29, 1995
ReceivedJul 25, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943603

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.