ClearanceBrief
510(k) K900884 ยท KGC Tube, Gastro-Enterostomy

P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY

ApplicantApplied Medical Technologies, Independence OH, US
DecisionUnknown, Jul 2, 1990
ReceivedFeb 26, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900884

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.