ClearanceBrief
510(k) K882025 ยท FMF Syringe, Piston

MODIFIED EXTRAVAKIT

ApplicantExtravakit, Inc., Tucson AZ, US
DecisionUnknown, Jul 27, 1988
ReceivedMay 17, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882025

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.