ClearanceBrief
510(k) K912444 ยท LGM Chamber, Patient Isolation

MICROBACT 12A SYSTEM, 12B SYSTEM, AND 24E SYSTEM

ApplicantRadiometer America, Inc., Westlake OH, US
DecisionSubstantially Equivalent, Feb 18, 1992
ReceivedJun 3, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912444

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.