ClearanceBrief
510(k) K940210 ยท EFQ Gauze/Sponge, Internal

VISITEC EYE PAD

ApplicantVisitec Co., Sarasota FL, US
DecisionSubstantially Equivalent, Mar 7, 1994
ReceivedJan 14, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940210

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.