ClearanceBrief
510(k) K880340 ยท INX Bed, Air Fluidized

MODIFIED AIR FLUIDIZED BED, KINAIR

ApplicantKinetic Concepts, Inc., San Antonio TX, US
DecisionSubstantially Equivalent, Feb 16, 1988
ReceivedJan 26, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880340

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.