FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

UDE

K Number: K202292 · Decision Oct 5, 2020
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
1
Review Days
54

Basic Information

Device Name
UDE
K Number
K202292
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
EBM Technologies Inc.
Date Received
August 12, 2020
Decision Date
October 5, 2020
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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