ClearanceBrief
510(k) K960309 ยท CAW Generator, Oxygen, Portable

AIRSEP NEWLIFE DUAL SIX OXYGEN CONCENTRATOR (MODIFICATION)

ApplicantAirsep Corp., Buffalo NY, US
DecisionSubstantially Equivalent, Feb 28, 1997
ReceivedJan 5, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960309

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.