ClearanceBrief
510(k) K862335 ยท

MODIFIED I.V. START, RE-START, PEDI AND GERI-KIT

ApplicantU.S. Mfg. & Management, Inc., San Bernardino CA, US
DecisionSubstantially Equivalent for Some Indications, Jul 24, 1986
ReceivedJun 19, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862335

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.