FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

Cetus system, Cetus probe

K Number: K170183 · Decision Sep 27, 2017
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
148
Applicant Total
6
Review Days
247

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Basic Information

Device Name
Cetus system, Cetus probe
K Number
K170183
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4150
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
A.R.C Laser GmbH
Date Received
January 23, 2017
Decision Date
September 27, 2017
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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K Number Device Name
K220531 FOX 810, FOX 980
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K091059 FOXQ 980 LASER
K073322 FOX 1-980, FOX Q-1064, FOX-Q-810