LiquID .051 LP Guide Catheter Extension
K-Number: K243691 · 2025-04-04
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.