MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122— 510(k) K040228

Name: FDA 510(k) clearance K040228
Creator: U.S. Food and Drug Administration
Published: 2004-04-29

Substantially Equivalent

Medi-Stim A/S

FDA 510(k) clearance K040228 for MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122, Substantially Equivalent on 2004-04-29. Applicant: Medi-Stim A/S. Device class: 2.

Clearance details

Applicant: Medi-Stim A/S
Product code: Code DPW
Device class: Class 2
Regulation: 21 CFR 870.2100
Advisory panel: Cardiovascular
Date received: 2004-02-02
Decision date: 2004-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brooklyn Park, MN, US

Download summary PDF View on FDA.gov ↗

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Recalls naming K040228

K-number listed on FDA's recall record

Z-0719-2018 — MEDISTIM VERIQ SYSTEM, MODEL VQ4122 An intraoperative diagnostic system that utilizes ultrasonography to guide surgeons to successfully plan and accomplish surgical interventions.Class II·Terminated·Medistim Asa·20170425

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K040228.

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