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FDA 510(k)

LiquID .051 LP Guide Catheter Extension

K-Number: K243691 · 2025-04-04

Decision Date2025-04-04
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LiquID .051 LP Guide Catheter Extension is a medical device manufactured by Seigla Medical, Inc.. It received FDA 510(k) clearance on 2025-04-04 under approval number K243691. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LiquID .051 LP Guide Catheter Extension?

LiquID .051 LP Guide Catheter Extension is a medical device that received FDA 510(k) clearance on 2025-04-04. It is manufactured by Seigla Medical, Inc.. The 510(k) number is K243691.

When was LiquID .051 LP Guide Catheter Extension approved by the FDA?

LiquID .051 LP Guide Catheter Extension received FDA 510(k) clearance on 2025-04-04, under approval number K243691.

What company makes LiquID .051 LP Guide Catheter Extension?

LiquID .051 LP Guide Catheter Extension is manufactured by Seigla Medical, Inc..

What is the FDA product code for LiquID .051 LP Guide Catheter Extension?

The FDA product code for LiquID .051 LP Guide Catheter Extension is DQY.

Related Clinical Trials

Other Devices by Seigla Medical, Inc.

Related Devices (Code: DQY)

Official Source

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