FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

RAYSCAN a-Expert3D

K Number: K232287 · Decision Aug 31, 2023
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
24
Review Days
30

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Basic Information

Device Name
RAYSCAN a-Expert3D
K Number
K232287
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ray Co., Ltd.
Date Received
August 1, 2023
Decision Date
August 31, 2023
Product Code
OAS
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
OAS X-Ray, Tomography, Computed, Dental

Similar 510(k) Clearances

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Other Clearances by Ray Co., Ltd.

K Number Device Name
K260462 RCT800
K251798 RCT700
K251109 SMARTDent
K243903 RCT600
K233625 RAYDENT SW
K232325 RAYSCAN a-Expert
K230753 RCT800
K213226 RCT700
K211105 Ear-Friendly Mask
K192737 RCT800
Search all 24 clearances from Ray Co., Ltd. →