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FDA 510(k)

MEDIC4ALL TELEMEDICINE SYSTEM VMS-01

K-Number: K061502 · 2006-09-15

Decision Date2006-09-15
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDIC4ALL TELEMEDICINE SYSTEM VMS-01 is the device name listed in this FDA 510(k) record. The listed applicant is Medic4all (Israel) , Ltd.. It received FDA 510(k) clearance on 2006-09-15 under 510(k) number K061502. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIC4ALL TELEMEDICINE SYSTEM VMS-01?

MEDIC4ALL TELEMEDICINE SYSTEM VMS-01 is a medical device that received FDA 510(k) clearance on 2006-09-15. The listed applicant is Medic4all (Israel) , Ltd.. The 510(k) number is K061502.

When did MEDIC4ALL TELEMEDICINE SYSTEM VMS-01 receive FDA 510(k) clearance?

MEDIC4ALL TELEMEDICINE SYSTEM VMS-01 received FDA 510(k) clearance on 2006-09-15, under 510(k) number K061502.

Who is the listed applicant for MEDIC4ALL TELEMEDICINE SYSTEM VMS-01?

The FDA 510(k) record lists Medic4all (Israel) , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDIC4ALL TELEMEDICINE SYSTEM VMS-01?

The FDA product code for MEDIC4ALL TELEMEDICINE SYSTEM VMS-01 is DRG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medic4all (Israel) , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: DRG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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