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FDA 510(k)

VIVO

K-Number: K183195 · 2019-06-14

ApplicantCatheter Precision, Inc.
Decision Date2019-06-14
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VIVO is a medical device manufactured by Catheter Precision, Inc.. It received FDA 510(k) clearance on 2019-06-14 under approval number K183195. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIVO?

VIVO is a medical device that received FDA 510(k) clearance on 2019-06-14. It is manufactured by Catheter Precision, Inc.. The 510(k) number is K183195.

When was VIVO approved by the FDA?

VIVO received FDA 510(k) clearance on 2019-06-14, under approval number K183195.

What company makes VIVO?

VIVO is manufactured by Catheter Precision, Inc..

What is the FDA product code for VIVO?

The FDA product code for VIVO is DQK.

Other Devices by Catheter Precision, Inc.

K200313VIVO

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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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