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

QEVO System

K Number: K232159 · Decision Sep 21, 2023
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
92
Applicant Total
45
Review Days
63

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Basic Information

Device Name
QEVO System
K Number
K232159
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.1480
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carl Zeiss Meditec, AG
Date Received
July 20, 2023
Decision Date
September 21, 2023
Product Code
GWG
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWG Endoscope, Neurological

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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
K231676 CALLISTO eye
K230858 QUATERA 700
K213527 FORUM
K211346 BLUE 400
K212241 QUATERA 700
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