Vista Clear— 510(k) K193389

Name: FDA 510(k) clearance K193389
Creator: U.S. Food and Drug Administration
Published: 2020-03-04

Substantially Equivalent

Inter-Med/Vista Dental Products

FDA 510(k) clearance K193389 for Vista Clear, Substantially Equivalent on 2020-03-04. Applicant: Inter-Med/Vista Dental Products. Device class: Unclassified.

Clearance details

Applicant: Inter-Med/Vista Dental Products
Product code: Code MVL
Device class: Unclassified
Advisory panel: Unknown
Date received: 2019-12-06
Decision date: 2020-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Racine, WI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MVL

view all

K254239 — CyClean Cord2026-03-27
K253797 — One-Stop2026-02-27
K243910 — Retraxil2025-09-24
K211420 — Stasis Gel2022-03-14
K211419 — Gingi-Aid Gel2022-01-10

More clearances from Inter-Med/Vista Dental Products

view all

K193357 — V-Mix2020-10-23
K193409 — Vista Rinse, Vista Rinse Plus2020-09-09
K193447 — Vista Dyes2020-03-11
K190220 — Vista FS, Vista FS Liquid2019-06-10
K170101 — Valiant Curing Light2017-06-08

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