FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

FDR Cross (DR-XD 3000)

K Number: K212956 · Decision Nov 8, 2021
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
64
Review Days
53

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Basic Information

Device Name
FDR Cross (DR-XD 3000)
K Number
K212956
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fujifilm Corporation
Date Received
September 16, 2021
Decision Date
November 8, 2021
Product Code
OWB
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
OWB Interventional Fluoroscopic X-Ray System

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