ClearanceBrief
510(k) K960833 ยท FRA Purifier, Air, Ultraviolet, Medical

VIOTEC S-4000-CR SECURITY SERIES ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM

ApplicantUv Technologies, Inc., West Cadwell NJ, US
DecisionSubstantially Equivalent, Jul 25, 1996
ReceivedFeb 29, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960833

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.