FDA 510(k)
FDA class 2
Substantially Equivalent
🇫🇷 France
Volta AF-Xplorer
K Number: K243812
·
Decision May 9, 2025
Classifications
1
FEI Numbers
178
Registration Numbers
178
Same Product Code
429
Applicant Total
5
Review Days
149
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Basic Information
- Device Name
- Volta AF-Xplorer
- K Number
- K243812
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1425
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Volta Medical
- Date Received
- December 11, 2024
- Decision Date
- May 9, 2025
- Product Code
- DQK
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DQK | Computer, Diagnostic, Programmable | FDA class 2 | Cardiovascular |
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