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

AS-10

K Number: K200887 · Decision Apr 15, 2020
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
43
Review Days
13

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Basic Information

Device Name
AS-10
K Number
K200887
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Canon, Inc.
Date Received
April 2, 2020
Decision Date
April 15, 2020
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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