FDA 510(k)
FDA class 2
Substantially Equivalent
🇰🇷 South Korea
DT-703
K Number: K221233
·
Decision Jun 27, 2022
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
189
Applicant Total
4
Review Days
59
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Basic Information
- Device Name
- DT-703
- K Number
- K221233
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.1800
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ecotron Co., Ltd.
- Date Received
- April 29, 2022
- Decision Date
- June 27, 2022
- Product Code
- EHD
- 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 |
|---|---|---|---|
| EHD | Unit, X-Ray, Extraoral With Timer | FDA class 2 | Dental |
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Other Clearances by Ecotron Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K180473 | ANYVIEW DR SERIES FPD Fluoroscopic Mobile C-arm ANYVIEW-240DR, ANYVIEW-320DR, ANYVIEW-500DR | Mar 23, 2018 | Substantially Equivalent |
| K160279 | ANYVIEW-500R Fluoroscopic Mobile X-Ray System | Oct 14, 2016 | Substantially Equivalent |
| K151038 | EPX-Series Mobile X-ray System | Jul 24, 2015 | Substantially Equivalent |