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FDA 510(k)

LILY Extension Tube and Needleless Connector

K-Number: K222780 · 2023-11-09

ApplicantLily Medical Corporation
Decision Date2023-11-09
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LILY Extension Tube and Needleless Connector is a medical device manufactured by Lily Medical Corporation. It received FDA 510(k) clearance on 2023-11-09 under approval number K222780. 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 LILY Extension Tube and Needleless Connector?

LILY Extension Tube and Needleless Connector is a medical device that received FDA 510(k) clearance on 2023-11-09. It is manufactured by Lily Medical Corporation. The 510(k) number is K222780.

When was LILY Extension Tube and Needleless Connector approved by the FDA?

LILY Extension Tube and Needleless Connector received FDA 510(k) clearance on 2023-11-09, under approval number K222780.

What company makes LILY Extension Tube and Needleless Connector?

LILY Extension Tube and Needleless Connector is manufactured by Lily Medical Corporation.

What is the FDA product code for LILY Extension Tube and Needleless Connector?

The FDA product code for LILY Extension Tube and 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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