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

CANON Fundus Camera CR-10 (CR-10)

K Number: K241049 · Decision May 15, 2024
Classifications
1
FEI Numbers
67
Registration Numbers
68
Same Product Code
151
Applicant Total
14
Review Days
28

Basic Information

Device Name
CANON Fundus Camera CR-10 (CR-10)
K Number
K241049
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
886.1120
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Canon Inc.
Date Received
April 17, 2024
Decision Date
May 15, 2024
Product Code
HKI
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HKI Camera, Ophthalmic, Ac-Powered

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