ClearanceBrief
510(k) K881150 ยท GIS Test, Fibrinogen

KINETIC FIBRINOGEN ASSAY

ApplicantBio/Data Corp., Hatboro PA, US
DecisionSubstantially Equivalent, Mar 28, 1988
ReceivedMar 17, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881150

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.