FDA 510(k)
FDA class 2
Substantially Equivalent
🇰🇷 South Korea
E-CUBE 15
K Number: K121888
·
Decision Jul 26, 2012
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
26
Review Days
28
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Basic Information
- Device Name
- E-CUBE 15
- K Number
- K121888
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1560
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Alpinion Medical Systems Co., Ltd.
- Date Received
- June 28, 2012
- Decision Date
- July 26, 2012
- Product Code
- IYO
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| IYO | System, Imaging, Pulsed Echo, Ultrasonic | FDA class 2 | Radiology |
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Other Clearances by Alpinion Medical Systems Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K223564 | X-CUBE 50, X-CUBE 60 | Apr 17, 2023 | Substantially Equivalent |
| K221093 | X-CUBE 70, X-CUBE 90 | Oct 14, 2022 | Substantially Equivalent |
| K220857 | X-CUBE 50, X-CUBE 60 | Oct 13, 2022 | Substantially Equivalent |
| K213523 | X-CUBE i8, X-CUBE i9 | Jan 28, 2022 | Substantially Equivalent |
| K211300 | X-CUBE 90 | Aug 9, 2021 | Substantially Equivalent |
| K211299 | X-CUBE 70 | Aug 9, 2021 | Substantially Equivalent |
| K200450 | X-Cube 70 | Jul 10, 2020 | Substantially Equivalent |
| K200449 | X-Cube 90 | Jul 10, 2020 | Substantially Equivalent |
| K182594 | E-CUBE i7 | Jan 24, 2019 | Substantially Equivalent |
| K182845 | minisono | Dec 27, 2018 | Substantially Equivalent |