Curapuls 670— 510(k) K243112
Substantially EquivalentEnraf-Nonius, B.V.
FDA 510(k) clearance K243112 for Curapuls 670, Substantially Equivalent on 2025-06-25. Applicant: Enraf-Nonius, B.V.. Device class: 2.
Clearance details
- Applicant
- Enraf-Nonius, B.V.
- Product code
- Code IMJ
- Device class
- Class 2
- Regulation
- 21 CFR 890.5290
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rotterdam, NL
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