ClearanceBrief
510(k) K884529 ยท INX Bed, Air Fluidized

MICROAIR FLUIDIZED AIR BED

ApplicantGsi Development Co., Carmel NY, US
DecisionSubstantially Equivalent, Nov 18, 1988
ReceivedOct 28, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884529

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.