510(k) K903462 · KYF Implant, Eye Valve

OPTIMED GLAUCOMA PRESSURE REGULATOR

Applicant	Optimed, Inc., Santa Barbara CA, US
Decision	Substantially Equivalent, Oct 16, 1990
Received	Aug 1, 1990
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K903462

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.