FDA 510(k)
FDA class 2
Substantially Equivalent
🇳🇱 Netherlands
Curapuls 670
K Number: K243112
·
Decision Jun 25, 2025
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
44
Applicant Total
5
Review Days
268
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Basic Information
- Device Name
- Curapuls 670
- K Number
- K243112
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.5290
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Enraf-Nonius, B.V.
- Date Received
- September 30, 2024
- Decision Date
- June 25, 2025
- Product Code
- IMJ
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| IMJ | Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat | FDA class 2 | Physical Medicine |
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Other Clearances by Enraf-Nonius, B.V.
| K Number | Device Name | ||
|---|---|---|---|
| K251083 | Compact II | Sep 12, 2025 | Substantially Equivalent |
| K230472 | Sonopuls 190 | Oct 24, 2023 | Substantially Equivalent |
| K151640 | ELTRAC 471 | Oct 16, 2015 | Substantially Equivalent |
| K030297 | FLEXIBLE RUBBER ELECTRODES, MODELS: 1460265, 1460272, 1460274, 3444128, 3444129, 3444130 | Apr 28, 2003 | Substantially Equivalent |