ClearanceBrief
510(k) K884342 ยท LIO Device, Specimen Collection

NOVAPATH SPECIMEN COLLECTION KIT

ApplicantBio-Rad, Hercules CA, US
DecisionSubstantially Equivalent, Nov 3, 1988
ReceivedOct 14, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884342

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.