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

Flash Ultrasound System 5100 Point of Care

K Number: K250030 · Decision Apr 28, 2025
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
1171
Applicant Total
23
Review Days
112

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Basic Information

Device Name
Flash Ultrasound System 5100 Point of Care
K Number
K250030
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Philips Ultrasound, LLC
Date Received
January 6, 2025
Decision Date
April 28, 2025
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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Other Clearances by Philips Ultrasound, LLC

K Number Device Name
K260123 EPIQ Series Diagnostic Ultrasound System
K260680 EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems
K252558 Lumify Diagnostic Ultrasound System
K253595 EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System
K252557 Lumify Diagnostic Ultrasound System
K251651 EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System
K251455 EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System
K250886 EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems
K243793 EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System
K251110 EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems
Search all 23 clearances from Philips Ultrasound, LLC →