ClearanceBrief
510(k) K850883 ยท HOZ Sponge, Ophthalmic

SCLERAL SPONGE II, OLK DESIGN, E5395-10 & E5395-11

ApplicantStorz Instrument Co., St. Louis MO, US
DecisionSubstantially Equivalent, Mar 20, 1985
ReceivedMar 4, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850883

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.