ClearanceBrief
510(k) K770605 ยท

TUBES, HYDROLYSIS, CALIBRATED

ApplicantOrganon, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 15, 1977
ReceivedMar 31, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770605

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.