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FDA 510(k)

TELEMEDICINE SYSTEM MODEL VMS-01

K-Number: K062662 · 2006-11-21

ApplicantMedic4all (Israel) , Ltd.
Decision Date2006-11-21
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TELEMEDICINE SYSTEM MODEL 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 2006-11-21 under 510(k) number K062662. 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 TELEMEDICINE SYSTEM MODEL VMS-01?

TELEMEDICINE SYSTEM MODEL VMS-01 is a medical device that received FDA 510(k) clearance on 2006-11-21. The listed applicant is Medic4all (Israel) , Ltd.. The 510(k) number is K062662.

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

TELEMEDICINE SYSTEM MODEL VMS-01 received FDA 510(k) clearance on 2006-11-21, under 510(k) number K062662.

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

The FDA product code for TELEMEDICINE SYSTEM MODEL 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K062127MEDIC4ALL TELEMEDICINE SYSTEM, MODEL VMS-01 (NIBP)K061502MEDIC4ALL TELEMEDICINE SYSTEM VMS-01

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.

K261569UbiqVue™ 2AYe Cardiac System (UX2253)Lifesignals, Inc.K252984Perin Health System (PHD80060-2)Perin Health Devices, LLCK252440EasyTeleMed (2.0.2)Ingeniars S.R.L.K250259TeleRehab Aermos Cardiopulmonary RehabilitationThe ScottCare CorporationK243837iBSMIorbit Digital Technologies Private LimitedK242018UbiqVue™ 2A Multi-parameter System (UX2550)Lifesignals, Inc.

Official Source

View on FDA Database →

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

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