FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Voluson SWIFT; Voluson SWIFT+

K Number: K230346 · Decision Jun 20, 2023
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
1171
Applicant Total
1
Review Days
132

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Basic Information

Device Name
Voluson SWIFT; Voluson SWIFT+
K Number
K230346
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ge Medical Systems Ultrasound & Primary Care Diagnostic, LLC
Date Received
February 8, 2023
Decision Date
June 20, 2023
Product Code
IYN
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
IYN System, Imaging, Pulsed Doppler, Ultrasonic

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