PainFreeze II— 510(k) K232674

Substantially Equivalent

Nuance 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
Download summary PDFView on FDA.gov ↗

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