ClearanceBrief
510(k) K831213 ยท JRE Refractometer For Clinical Use

SPECIFIC GRAVITY INSTRUMENT

ApplicantIris, Mchenry IL, US
DecisionSubstantially Equivalent, Jun 30, 1983
ReceivedApr 14, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831213

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.