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FDA 510(k)

VTRUST BLOOD PRESSURE MONITOR, MODEL VTRUST 701DH

K-Number: K091414 · 2009-10-21

ApplicantBiocare Corp.
Decision Date2009-10-21
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VTRUST BLOOD PRESSURE MONITOR, MODEL VTRUST 701DH is the device name listed in this FDA 510(k) record. The listed applicant is Biocare Corp.. It received FDA 510(k) clearance on 2009-10-21 under 510(k) number K091414. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VTRUST BLOOD PRESSURE MONITOR, MODEL VTRUST 701DH?

VTRUST BLOOD PRESSURE MONITOR, MODEL VTRUST 701DH is a medical device that received FDA 510(k) clearance on 2009-10-21. The listed applicant is Biocare Corp.. The 510(k) number is K091414.

When did VTRUST BLOOD PRESSURE MONITOR, MODEL VTRUST 701DH receive FDA 510(k) clearance?

VTRUST BLOOD PRESSURE MONITOR, MODEL VTRUST 701DH received FDA 510(k) clearance on 2009-10-21, under 510(k) number K091414.

Who is the listed applicant for VTRUST BLOOD PRESSURE MONITOR, MODEL VTRUST 701DH?

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

What is the FDA product code for VTRUST BLOOD PRESSURE MONITOR, MODEL VTRUST 701DH?

The FDA product code for VTRUST BLOOD PRESSURE MONITOR, MODEL VTRUST 701DH is DXN.

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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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