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 | Device Class | Medical Specialty |
|---|---|---|---|
| MUH | System, X-Ray, Extraoral Source, Digital | FDA class 2 | Dental |
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|---|---|---|---|
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| K243903 | RCT600 | Mar 12, 2025 | Substantially Equivalent |
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| K232287 | RAYSCAN a-Expert3D | Aug 31, 2023 | Substantially Equivalent |
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| K213226 | RCT700 | Nov 29, 2021 | Substantially Equivalent |
| K211105 | Ear-Friendly Mask | May 17, 2021 | Substantially Equivalent |