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FDA 510(k)

Intravascular Extension Sets and Accessories

K-Number: K192366 · 2020-07-20

ApplicantBaxter Healthcare Corporation
Decision Date2020-07-20
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Intravascular Extension Sets and Accessories is a medical device manufactured by Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2020-07-20 under approval number K192366. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Intravascular Extension Sets and Accessories?

Intravascular Extension Sets and Accessories is a medical device that received FDA 510(k) clearance on 2020-07-20. It is manufactured by Baxter Healthcare Corporation. The 510(k) number is K192366.

When was Intravascular Extension Sets and Accessories approved by the FDA?

Intravascular Extension Sets and Accessories received FDA 510(k) clearance on 2020-07-20, under approval number K192366.

What company makes Intravascular Extension Sets and Accessories?

Intravascular Extension Sets and Accessories is manufactured by Baxter Healthcare Corporation.

What is the FDA product code for Intravascular Extension Sets and Accessories?

The FDA product code for Intravascular Extension Sets and Accessories is FPA.

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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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