FDA 510(k)
FDA class 2
Substantially Equivalent
🇫🇷 France
Fetal EchoScan (v1.2)
K Number: K252294
·
Decision Dec 8, 2025
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
21
Applicant Total
5
Review Days
138
Basic Information
- Device Name
- Fetal EchoScan (v1.2)
- K Number
- K252294
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.2060
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Brightheart
- Date Received
- July 23, 2025
- Decision Date
- December 8, 2025
- Product Code
- POK
- 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 |
|---|---|---|---|
| POK | Computer-Assisted Diagnostic Software For Lesions Suspicious For Cancer | FDA class 2 | Radiology |
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