TELEMEDICINE SYSTEM MODEL VMS-01— 510(k) K062662

Name: FDA 510(k) clearance K062662
Creator: U.S. Food and Drug Administration
Published: 2006-11-21

Substantially Equivalent

Medic4all (Israel) , Ltd.

FDA 510(k) clearance K062662 for TELEMEDICINE SYSTEM MODEL VMS-01, Substantially Equivalent on 2006-11-21. Applicant: Medic4all (Israel) , Ltd.. Device class: 2.

Clearance details

Applicant: Medic4all (Israel) , Ltd.
Product code: Code DRG
Device class: Class 2
Regulation: 21 CFR 870.2910
Advisory panel: Cardiovascular
Date received: 2006-09-07
Decision date: 2006-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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More clearances from Medic4all (Israel) , Ltd.

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K062127 — MEDIC4ALL TELEMEDICINE SYSTEM, MODEL VMS-01 (NIBP)2006-11-08
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Adverse events under product code DRG

product code DRG

Death: 5
Total: 5

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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