ClearanceBrief
510(k) K072985 ยท KYB Lens, Guide, Intraocular

DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2

ApplicantDuckworth & Kent, Ltd., Baldock, Hertfordshire, GB
DecisionSubstantially Equivalent, Jun 20, 2008
ReceivedOct 23, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072985

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.