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

RCT800

K Number: K182805 · Decision Dec 14, 2018
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
24
Review Days
73

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Basic Information

Device Name
RCT800
K Number
K182805
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
October 2, 2018
Decision Date
December 14, 2018
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

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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
K232287 RAYSCAN a-Expert3D
K230753 RCT800
K213226 RCT700
K211105 Ear-Friendly Mask
Search all 24 clearances from Ray Co., Ltd. →