ClearanceBrief
510(k) K905703 ยท KYF Implant, Eye Valve

KRUPIN EYE VALVE WITH DISK

ApplicantHood Laboratories, Pembroke MA, US
DecisionSubstantially Equivalent, Mar 15, 1991
ReceivedDec 20, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905703

DateFirm and productCodeLinked 510(k)
May 6, 2006Eagle Vision Inc
Krupin Eye Valve, P/N 6003
Terminated
KYFNone listed
May 6, 2006Eagle Vision Inc
Glaucoma Aqueous Shunt, 209 mm, valved, P/N EG209V
Terminated
KYFNone listed
May 6, 2006Eagle Vision Inc
Glaucoma Aqueous Shunt 365 mm, valved, P/N EG365V
Terminated
KYFNone listed
May 6, 2006Eagle Vision Inc
Valve-EV Glaucoma Ultra-Smooth, P/N 6006
Terminated
KYFNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.