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FDA 510(k)

ClariVein IC

K-Number: K201907 · 2020-08-06

ApplicantMerit Medical Systems, Inc.
Decision Date2020-08-06
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ClariVein IC is a medical device manufactured by Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2020-08-06 under approval number K201907. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ClariVein IC?

ClariVein IC is a medical device that received FDA 510(k) clearance on 2020-08-06. It is manufactured by Merit Medical Systems, Inc.. The 510(k) number is K201907.

When was ClariVein IC approved by the FDA?

ClariVein IC received FDA 510(k) clearance on 2020-08-06, under approval number K201907.

What company makes ClariVein IC?

ClariVein IC is manufactured by Merit Medical Systems, Inc..

What is the FDA product code for ClariVein IC?

The FDA product code for ClariVein IC is KRA.

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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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