FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

INTRAOCULAR LENS GUIDE

K Number: K823222 · Decision Dec 28, 1982
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
38
Applicant Total
17
Review Days
60

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Basic Information

Device Name
INTRAOCULAR LENS GUIDE
K Number
K823222
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4300
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
American Medical Optics
Date Received
October 29, 1982
Decision Date
December 28, 1982
Product Code
KYB
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
KYB Lens, Guide, Intraocular

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KYB), ordered by most recent decision date.

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Other Clearances by American Medical Optics

K Number Device Name
K860001 BARRAQUER-KRUMEICH REFRACTIVE SET
K851263 AMER. MEDICAL OPTIC MONOCULAR DIRECT OPHTHALMASCOP
K851264 AMER. MEDICAL OPTICS MONOCULAR INDIRECT OPHTHALMAS
K851262 AMER. MEDICAL OPTICAL BINOCULAR INDIRECT OPHTHALMA
K844150 MEDICAL OPTICS PHACOEMULSIFICATION KIT
K843966 ARGON/KRYPTON LASER PHOTOCOAGULATOR SYS
K843965 ARGON LASER PHOTOCOAGULATOR SYS
K842197 AMERICAN MEDICAL OPTICS I/A KIT- IRRIG
K842504 AMER. MEDICAL OPTICS DIGITAL KERATO-
K842127 AMERICAN MEDICAL OPTICS IMAGING SYS
Search all 17 clearances from American Medical Optics →