ClearanceBrief
510(k) K896822 ยท FYD Apparatus, Exhaust, Surgical

SURGISMOKE

ApplicantSpectro Industries, Inc., Roseville MN, US
DecisionSubstantially Equivalent, Jan 11, 1990
ReceivedDec 4, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896822

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.