FDA 510(k)

VIVORTE BVF LITE

K-Number: K131133 · 2013-08-12

Decision Date2013-08-12

Product CodeMQV

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

VIVORTE BVF LITE is the device name listed in this FDA 510(k) record. The listed applicant is Vivorte, Inc.. It received FDA 510(k) clearance on 2013-08-12 under 510(k) number K131133. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIVORTE BVF LITE?

VIVORTE BVF LITE is a medical device that received FDA 510(k) clearance on 2013-08-12. The listed applicant is Vivorte, Inc.. The 510(k) number is K131133.

When did VIVORTE BVF LITE receive FDA 510(k) clearance?

VIVORTE BVF LITE received FDA 510(k) clearance on 2013-08-12, under 510(k) number K131133.

Who is the listed applicant for VIVORTE BVF LITE?

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

What is the FDA product code for VIVORTE BVF LITE?

The FDA product code for VIVORTE BVF LITE is MQV.

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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 Vivorte, Inc. as applicant

K130703VIVORTE BVF

Related Devices (Code: MQV)

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.