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FDA 510(k)

VAR MONITOR

K-Number: K073261 · 2008-05-23

ApplicantVortran Medical Technology 1, Inc.
Decision Date2008-05-23
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VAR MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Vortran Medical Technology 1, Inc.. It received FDA 510(k) clearance on 2008-05-23 under 510(k) number K073261. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAR MONITOR?

VAR MONITOR is a medical device that received FDA 510(k) clearance on 2008-05-23. The listed applicant is Vortran Medical Technology 1, Inc.. The 510(k) number is K073261.

When did VAR MONITOR receive FDA 510(k) clearance?

VAR MONITOR received FDA 510(k) clearance on 2008-05-23, under 510(k) number K073261.

Who is the listed applicant for VAR MONITOR?

The FDA 510(k) record lists Vortran Medical Technology 1, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAR MONITOR?

The FDA product code for VAR MONITOR is BTL.

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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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