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FDA 510(k)

Instylla Microcatheter

K-Number: K200744 · 2020-04-21

Decision Date2020-04-21
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Instylla Microcatheter is a medical device manufactured by Instylla, Inc.. It received FDA 510(k) clearance on 2020-04-21 under approval number K200744. 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 Instylla Microcatheter?

Instylla Microcatheter is a medical device that received FDA 510(k) clearance on 2020-04-21. It is manufactured by Instylla, Inc.. The 510(k) number is K200744.

When was Instylla Microcatheter approved by the FDA?

Instylla Microcatheter received FDA 510(k) clearance on 2020-04-21, under approval number K200744.

What company makes Instylla Microcatheter?

Instylla Microcatheter is manufactured by Instylla, Inc..

What is the FDA product code for Instylla Microcatheter?

The FDA product code for Instylla Microcatheter is KRA.

Other Devices by Instylla, Inc.

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Related Devices (Code: KRA)

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.