ClearanceBrief
510(k) K970788 ยท FHO Pneumoperitoneum Needle

PNEUMO-MATIC INSUFFLATION NEEDLE

ApplicantApple Medical Corp., Bolton MA, US
DecisionSubstantially Equivalent, Mar 27, 1997
ReceivedMar 4, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970788

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.