ClearanceBrief
510(k) K951894 ยท FHO Pneumoperitoneum Needle

ACCESS EXPANSION SYSTEM

ApplicantMicro-Medical Devices, Inc., Castle Pines Village CO, US
DecisionUnknown, Jun 15, 1995
ReceivedApr 24, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951894

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.