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

LANDERS 3 STRUT IRRIGATING VITRECTOMY LENS RING

K Number: K912253 · Decision Aug 7, 1991
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
50
Review Days
78

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Basic Information

Device Name
LANDERS 3 STRUT IRRIGATING VITRECTOMY LENS RING
K Number
K912253
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ocular Instruments, Inc.
Date Received
May 21, 1991
Decision Date
August 7, 1991
Product Code
HQE
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
HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

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Other Clearances by Ocular Instruments, Inc.

K Number Device Name
K014170 STAURENGHI WIDE FIELD SCANNING LASER LENS
K012096 DISPOSABLE VITRECTOMY LENS
K933976 MANDELKORN SUTURE LYSIS LENS
K933264 RITCH NYLON SUTURE LASER LENS
K941420 50 DEGREE HRI PRISM LENS
K935302 OSHER SURGICAL GONIO/POSTERIOR POLE LENS
K921414 TROKEL /3 GONIO LASER LENS
K923670 BYRNE EXPULSIVE LENS
K914051 PEDIATRIC VITRECTOMY LENS SET
K914117 LANDERS HIGH REFRACTIVE INDEX VITRECTOMY LENS SET
Search all 50 clearances from Ocular Instruments, Inc. →