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

BARRAQUER-KRUMEICH REFRACTIVE SET

K Number: K860001 · Decision Feb 4, 1986
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
82
Applicant Total
17
Review Days
33

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Basic Information

Device Name
BARRAQUER-KRUMEICH REFRACTIVE SET
K Number
K860001
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4370
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
American Medical Optics
Date Received
January 2, 1986
Decision Date
February 4, 1986
Product Code
HNO
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
HNO Keratome, Ac-Powered

Similar 510(k) Clearances

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

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Other Clearances by American Medical Optics

K Number Device Name
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
K842250 AMER. MEDICAL OPTICS ARGON/KRYPTON LASE
Search all 17 clearances from American Medical Optics →