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FDA 510(k)

MEDVIZERTM VITELCARE PATIENT MONITORING SYSTEM

K-Number: K040581 · 2004-05-27

ApplicantVitel Net
Decision Date2004-05-27
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDVIZERTM VITELCARE PATIENT MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vitel Net. It received FDA 510(k) clearance on 2004-05-27 under 510(k) number K040581. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDVIZERTM VITELCARE PATIENT MONITORING SYSTEM?

MEDVIZERTM VITELCARE PATIENT MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2004-05-27. The listed applicant is Vitel Net. The 510(k) number is K040581.

When did MEDVIZERTM VITELCARE PATIENT MONITORING SYSTEM receive FDA 510(k) clearance?

MEDVIZERTM VITELCARE PATIENT MONITORING SYSTEM received FDA 510(k) clearance on 2004-05-27, under 510(k) number K040581.

Who is the listed applicant for MEDVIZERTM VITELCARE PATIENT MONITORING SYSTEM?

The FDA 510(k) record lists Vitel Net as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDVIZERTM VITELCARE PATIENT MONITORING SYSTEM?

The FDA product code for MEDVIZERTM VITELCARE PATIENT MONITORING SYSTEM is DQA.

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.

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Other records listing Vitel Net 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.

K000557MEDVIZER PACS, MODEL RELEASE 2000

Related Devices (Code: DQA)

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.

K252821Reusable Adult SpO2 Clip Sensor (3m) (M1196A); Reusable Adult SpO2 Clip Sensor (0.9m) (M1196T)Philips Medizin Systeme Böblingen GmbHK252655Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT, PO-C6AO, PO-C6AT)Shenzhen Imdk Medical Technology Co., Ltd.K253887Nasal Alar SpO2 Sensor (989803205381); Nasal Alar SpO2 Sensor (989803205391); Nasal Alar Sp02 Sensor (989803205401)Philips Medizin SystemeK260931Unimed Reusable Finger Clip SpO2 Sensors (U403-49R and U103-49R)Unimed Medical Supplies, Inc.K252448AViTA Pulse Oximeter (SP61)Avita CorporationK252805YUWELL® Finger Pulse Oximeter (YX105, YX106, YX110, YX310)Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

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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