FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

KRUPIN EYE VALVE WITH DISK

K Number: K905703 · Decision Mar 15, 1991
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
24
Applicant Total
19
Review Days
85

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Basic Information

Device Name
KRUPIN EYE VALVE WITH DISK
K Number
K905703
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.3920
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Hood Laboratories
Date Received
December 20, 1990
Decision Date
March 15, 1991
Product Code
KYF
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KYF Implant, Eye Valve

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K Number Device Name
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K897049 GIBSON ENDOLYMPHATIC SHUNT
K897059 HOOD SPEAKING VALVE
K893866 HOOD PEDIATRIC TRACHEOSTOMY TUBE
K884810 SILICONE LARYNGEAL STENT
K890599 HOOD NASAL SPLINT
K885125 KRUPIN EYE VALVE W/SCLERAL BUCKLE
K882430 HOOD TRACHEAL STOMA BUTTON
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