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

IOLMaster 700

K Number: K170171 · Decision Apr 6, 2017
Classifications
1
FEI Numbers
54
Registration Numbers
55
Same Product Code
107
Applicant Total
45
Review Days
77

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Basic Information

Device Name
IOLMaster 700
K Number
K170171
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1850
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carl Zeiss Meditec, AG
Date Received
January 19, 2017
Decision Date
April 6, 2017
Product Code
HJO
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
HJO Biomicroscope, Slit-Lamp, Ac-Powered

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Other Clearances by Carl Zeiss Meditec, AG

K Number Device Name
K241174 INTRABEAM (700); And accessories (INTRABEAM SMART Stand, INTRABEAM SMART Spherical Applicator, INTRABEAM Spherical Sizer Set, INTRABEAM Needle Applicator)
K233911 VISULAS combi
K240215 BLUE 400; BLUE 400 S
K233421 RESCAN 700
K232944 CALLISTO eye
K232159 QEVO System
K231676 CALLISTO eye
K230858 QUATERA 700
K213527 FORUM
K211346 BLUE 400
Search all 45 clearances from Carl Zeiss Meditec, AG →