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FDA 510(k)

VITALWARE VMS

K-Number: K050128 · 2005-05-13

ApplicantTelevital, Inc.
Decision Date2005-05-13
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITALWARE VMS is the device name listed in this FDA 510(k) record. The listed applicant is Televital, Inc.. It received FDA 510(k) clearance on 2005-05-13 under 510(k) number K050128. 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 VITALWARE VMS?

VITALWARE VMS is a medical device that received FDA 510(k) clearance on 2005-05-13. The listed applicant is Televital, Inc.. The 510(k) number is K050128.

When did VITALWARE VMS receive FDA 510(k) clearance?

VITALWARE VMS received FDA 510(k) clearance on 2005-05-13, under 510(k) number K050128.

Who is the listed applicant for VITALWARE VMS?

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

What is the FDA product code for VITALWARE VMS?

The FDA product code for VITALWARE VMS is DRG.

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Related Devices (Code: DRG)

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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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