ClearanceBrief
510(k) K885232 ยท HOZ Sponge, Ophthalmic

FLUID DRAINAGE WICK

ApplicantVisitec Co., Sarasota FL, US
DecisionSubstantially Equivalent, Feb 8, 1989
ReceivedDec 20, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K885232

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.