ClearanceBrief
510(k) K881380 ยท JSP Kit, Anaerobic Identification

B. FRAGTEX

ApplicantAmerican Biomedical Products, Inc., Tulsa OK, US
DecisionSubstantially Equivalent, Oct 6, 1988
ReceivedApr 1, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881380

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.