ClearanceBrief
510(k) K874244 ยท JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

DYNATECH MR 300 MANUAL MICROELISA

ApplicantDynatech Laboratories, Inc., Chantilly VA, US
DecisionSubstantially Equivalent, Nov 3, 1987
ReceivedOct 16, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874244

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.