ClearanceBrief
510(k) K827847 ยท

ARGON FIBER OPTIC CATHETER

ApplicantHgm, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Jan 3, 1983
ReceivedNov 4, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K827847

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.