FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

RAYSCAN A-EXPERT

K Number: K122918 · Decision Mar 15, 2013
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
205
Applicant Total
24
Review Days
172

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Basic Information

Device Name
RAYSCAN A-EXPERT
K Number
K122918
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ray Co., Ltd.
Date Received
September 24, 2012
Decision Date
March 15, 2013
Product Code
MUH
Advisory Committee
Dental
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
MUH System, X-Ray, Extraoral Source, Digital

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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. →