ClearanceBrief
510(k) K910463 ยท BTR Tube, Tracheal (W/Wo Connector)

MEROCEL(R) LASER-GUARD(TM)

ApplicantMerocel Corp., Mystic CT, US
DecisionSubstantially Equivalent, Apr 6, 1992
ReceivedJan 25, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910463

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.