510(k) K821897 · KYG Device, Irrigation, Ocular Surgery

LENS

Applicant	Mortan, Inc., Mchenry IL, US
Decision	Substantially Equivalent, Jan 5, 1983
Received	Jun 28, 1982
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K821897

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.