PainFreeze II— 510(k) K232674
Substantially EquivalentNuance Medical, LLC
FDA 510(k) clearance K232674 for PainFreeze II, Substantially Equivalent on 2024-02-12. Applicant: Nuance Medical, LLC. Device class: Unclassified.
Clearance details
- Applicant
- Nuance Medical, LLC
- Product code
- Code MLY
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Carlsbad, CA, US
Recent devices under product code MLY
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Data sourced from openFDA. This site is unofficial and independent of the FDA.