SDF Pro— 510(k) K250222

Substantially Equivalent

Belport Company, Inc., Gingi-Pak

FDA 510(k) clearance K250222 for SDF Pro, Substantially Equivalent on 2025-05-07. Applicant: Belport Company, Inc., Gingi-Pak. Device class: 2.

Clearance details

Applicant: Belport Company, Inc., Gingi-Pak
Product code: Code PHR
Device class: Class 2
Regulation: 21 CFR 872.3260
Advisory panel: Dental
Date received: 2025-01-27
Decision date: 2025-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Belport Company, Inc., Gingi-Pak

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Data sourced from openFDA. This site is unofficial and independent of the FDA.