ClearanceBrief
510(k) K900857 ยท FMF Syringe, Piston

NON STERILE PARENTERAL SUPPLY KIT

ApplicantIntermed, Inc., Sparta NJ, US
DecisionUnknown, May 22, 1990
ReceivedFeb 23, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900857

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.