RC-SwiftPrep— 510(k) K250279

Name: FDA 510(k) clearance K250279
Creator: U.S. Food and Drug Administration
Published: 2025-07-02

Substantially Equivalent

Belport Company, Inc., Gingi-Pak

FDA 510(k) clearance K250279 for RC-SwiftPrep, Substantially Equivalent on 2025-07-02. Applicant: Belport Company, Inc., Gingi-Pak. Device class: Unclassified.

Clearance details

Applicant: Belport Company, Inc., Gingi-Pak
Product code: Product code KJJ
Device class: Unclassified
Advisory panel: Unknown
Date received: 2025-01-31
Decision date: 2025-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KJJ

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K241354 — Sealer Solvent2024-08-27
K201785 — EPIEN Dental Cleanser2021-09-09
K211813 — Triton2021-08-18
K193357 — V-Mix2020-10-23
K193409 — Vista Rinse, Vista Rinse Plus2020-09-09

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

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K260430 — Porcelain Etch Gel2026-04-10
K251775 — RODIN Cement2025-09-02
K250222 — SDF Pro2025-05-07
K240688 — RODIN Titan 3D Resin2024-06-20
K231060 — ProMin Dental Desensitizing Gel2024-06-13

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