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FDA 510(k)

Needleless Connector

K-Number: K210217 · 2021-05-17

ApplicantJiangsu Caina Medical Co.,Ltd
Decision Date2021-05-17
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Needleless Connector is a medical device manufactured by Jiangsu Caina Medical Co.,Ltd. It received FDA 510(k) clearance on 2021-05-17 under approval number K210217. 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 Needleless Connector?

Needleless Connector is a medical device that received FDA 510(k) clearance on 2021-05-17. It is manufactured by Jiangsu Caina Medical Co.,Ltd. The 510(k) number is K210217.

When was Needleless Connector approved by the FDA?

Needleless Connector received FDA 510(k) clearance on 2021-05-17, under approval number K210217.

What company makes Needleless Connector?

Needleless Connector is manufactured by Jiangsu Caina Medical Co.,Ltd.

What is the FDA product code for Needleless Connector?

The FDA product code for Needleless Connector 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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