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

AT 030

K Number: K180839 · Decision Jun 7, 2018
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
55
Applicant Total
45
Review Days
69

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Basic Information

Device Name
AT 030
K Number
K180839
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1930
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carl Zeiss Meditec, AG
Date Received
March 30, 2018
Decision Date
June 7, 2018
Product Code
HKY
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
HKY Tonometer, Manual

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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
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