ClearanceBrief
510(k) K952610 ยท FNM Mattress, Air Flotation, Alternating Pressure

PLEXUS/3000 (P/3000), PLEXUS/3500 (P/3500)

ApplicantPlexus Medical, Glendora CA, US
DecisionSubstantially Equivalent, Sep 13, 1995
ReceivedJun 7, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952610

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.