FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

MP-1 MICROPERIMETER

K Number: K061768 · Decision Sep 28, 2006
Classifications
1
FEI Numbers
65
Registration Numbers
66
Same Product Code
155
Applicant Total
5
Review Days
97

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Basic Information

Device Name
MP-1 MICROPERIMETER
K Number
K061768
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1120
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nidek Technologies Srl
Date Received
June 23, 2006
Decision Date
September 28, 2006
Product Code
HKI
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
HKI Camera, Ophthalmic, Ac-Powered

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Other Clearances by Nidek Technologies Srl

K Number Device Name
K113451 NON-MYDRIATIC AUTO FUNDUS CAMERA AFC-330 WITH IMAGE FILING SOFTWARE NA VIS-EX
K070231 ORION
K023719 MP-1 MICRO PERIMETER
K012416 CONFOSCAN 2 CONFOCAL MICROSCOPE