ClearanceBrief
510(k) K030802 ยท LFD Saliva, Artificial

CAPHOSOL

ApplicantInpharma A.S., Northborough MA, US
DecisionSubstantially Equivalent, Nov 25, 2003
ReceivedMar 13, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030802

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.