FDA 510(k) FDA class 2 Substantially Equivalent 🇧🇪 Belgium

DR 100s

K Number: K191884 · Decision Aug 9, 2019
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
235
Applicant Total
6
Review Days
25

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Basic Information

Device Name
DR 100s
K Number
K191884
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1720
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Agfa N.V.
Date Received
July 15, 2019
Decision Date
August 9, 2019
Product Code
IZL
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
IZL System, X-Ray, Mobile

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