KRUPIN EYE VALVE W/SCLERAL BUCKLE

K885125 · Hood Laboratories · KYF · Jan 24, 1989 · Ophthalmic

Device Facts

Record IDK885125
Device NameKRUPIN EYE VALVE W/SCLERAL BUCKLE
ApplicantHood Laboratories
Product CodeKYF · Ophthalmic
Decision DateJan 24, 1989
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 886.3920
Device ClassClass 2

Regulatory Classification

Identification

An aqueous shunt is an implantable device intended to reduce intraocular pressure in the anterior chamber of the eye in patients with neovascular glaucoma or with glaucoma when medical and conventional surgical treatments have failed.

Special Controls

*Classification.* Class II. The special controls for this device are FDA's:(1) “Use of International Standard ISO 10993 ‘Biological Evaluation of Medical Devices—Part I: Evaluation and Testing,’ ” (2) “510(k) Sterility Review Guidance of 2/12/90 (K90-1),” and (3) “Aqueous Shunts—510(k) Submissions.”

Innolitics

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