FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

StarGuide

K Number: K210173 · Decision Mar 29, 2021
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
459
Applicant Total
47
Review Days
66

Basic Information

Device Name
StarGuide
K Number
K210173
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1200
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Healthcare
Date Received
January 22, 2021
Decision Date
March 29, 2021
Product Code
KPS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
KPS System, Tomography, Computed, Emission

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K Number Device Name
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K213689 Voluson P6, Voluson P8
K213642 Voluson S6, Voluson S8, Voluson S8t, Voluson S10, Voluson S10 Expert
K211488 LOGIQ E10
K211524 LOGIQ E10s, LOGIQ Fortis
K212004 MyoSPECT, MyoSpect ES
K211725 Senographe Pristina
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