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FDA 510(k)

VITALLINK3 MOBILE VITAL SIGNS SYSTEM

K-Number: K073094 · 2008-01-04

ApplicantTelemedic Systems, Ltd.
Decision Date2008-01-04
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITALLINK3 MOBILE VITAL SIGNS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Telemedic Systems, Ltd.. It received FDA 510(k) clearance on 2008-01-04 under 510(k) number K073094. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALLINK3 MOBILE VITAL SIGNS SYSTEM?

VITALLINK3 MOBILE VITAL SIGNS SYSTEM is a medical device that received FDA 510(k) clearance on 2008-01-04. The listed applicant is Telemedic Systems, Ltd.. The 510(k) number is K073094.

When did VITALLINK3 MOBILE VITAL SIGNS SYSTEM receive FDA 510(k) clearance?

VITALLINK3 MOBILE VITAL SIGNS SYSTEM received FDA 510(k) clearance on 2008-01-04, under 510(k) number K073094.

Who is the listed applicant for VITALLINK3 MOBILE VITAL SIGNS SYSTEM?

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

What is the FDA product code for VITALLINK3 MOBILE VITAL SIGNS SYSTEM?

The FDA product code for VITALLINK3 MOBILE VITAL SIGNS SYSTEM is MWI.

Related Clinical Trials

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Related Devices (Code: MWI)

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.

K260438Vital Signs Monitor (CLEO2)Infinium Medical, Inc.K253417Masimo Root Monitoring SystemMasimo CorporationK253196Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)Midmark CorporationK253436c-med0 alphaCosinuss GmbHK250135WAVE Clinical Platform (2.0.000)Baxter Healthcare Corp/ Excel MedicalK241766QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid)Fysicon BV

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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