ClearanceBrief
510(k) K883065 ยท KIT Media And Components, Synthetic Cell And Tissue Culture

ALLOPREP SYSTEM

ApplicantOsteotech, Inc., Shrewsbury NJ, US
DecisionSubstantially Equivalent, Oct 13, 1988
ReceivedJul 20, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883065

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.