ClearanceBrief
510(k) K802999 ยท JHI Visual, Pregnancy Hcg, Prescription Use

BETA-TEC QUALITATIVE

ApplicantArmkel, LLC, Mchenry IL, US
DecisionSubstantially Equivalent, Dec 22, 1980
ReceivedNov 25, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802999

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.