FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

Pocket III

K Number: K232302 · Decision Apr 26, 2024
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
30
Review Days
269

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Basic Information

Device Name
Pocket III
K Number
K232302
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Quantel Medical
Date Received
August 1, 2023
Decision Date
April 26, 2024
Product Code
IYO
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
IYO System, Imaging, Pulsed Echo, Ultrasonic

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