Gingi-Aid Gel— 510(k) K211419

Name: FDA 510(k) clearance K211419
Creator: U.S. Food and Drug Administration
Published: 2022-01-10

Substantially Equivalent

Belport Company, Inc., Gingi-Pak

FDA 510(k) clearance K211419 for Gingi-Aid Gel, Substantially Equivalent on 2022-01-10. Applicant: Belport Company, Inc., Gingi-Pak. Device class: Unclassified.

Clearance details

Applicant: Belport Company, Inc., Gingi-Pak
Product code: Code MVL
Device class: Unclassified
Advisory panel: Unknown
Date received: 2021-05-07
Decision date: 2022-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

Download summary PDF View on FDA.gov ↗

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