Vista FS, Vista FS Liquid— 510(k) K190220

Name: FDA 510(k) clearance K190220
Creator: U.S. Food and Drug Administration
Published: 2019-06-10

Substantially Equivalent

Inter-Med/Vista Dental Products

FDA 510(k) clearance K190220 for Vista FS, Vista FS Liquid, Substantially Equivalent on 2019-06-10. 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: 2019-02-05
Decision date: 2019-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Racine, WI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MVL

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More clearances from Inter-Med/Vista Dental Products

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K193357 — V-Mix2020-10-23
K193409 — Vista Rinse, Vista Rinse Plus2020-09-09
K193447 — Vista Dyes2020-03-11
K193389 — Vista Clear2020-03-04
K170101 — Valiant Curing Light2017-06-08

Recalls naming K190220

K-number listed on FDA's recall record

Z-2400-2026 — Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28Class II·Ongoing·Inter-Med Llc·20260527

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K190220.

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