ClearanceBrief
510(k) K962822 ยท CAF Nebulizer (Direct Patient Interface)

OPTICHAMBER

ApplicantHealthscan Products, Inc., Cedar Grove NJ, US
DecisionSubstantially Equivalent, Oct 17, 1996
ReceivedJul 19, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962822

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.