Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension

K-Number: K220691 · 2022-05-05

ApplicantSeigla Medical, Inc.
Decision Date2022-05-05
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension is a medical device manufactured by Seigla Medical, Inc.. It received FDA 510(k) clearance on 2022-05-05 under approval number K220691. 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 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension?

LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension is a medical device that received FDA 510(k) clearance on 2022-05-05. It is manufactured by Seigla Medical, Inc.. The 510(k) number is K220691.

When was LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension approved by the FDA?

LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension received FDA 510(k) clearance on 2022-05-05, under approval number K220691.

What company makes LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension?

LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension is manufactured by Seigla Medical, Inc..

What is the FDA product code for LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension?

The FDA product code for LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension is DQY.

Related Clinical Trials

NCT02193425 Reliability of the Human Brain Connectome COMPLETED NCT06958731 In-plane Versus Real Time Bi-plane Single-operator Laser-assisted With a Innovative T-shaped Probe for Ultrasound-guided Internal Jugular Vein Catheterization:A Randomized Controlled Trial ENROLLING_BY_INVITATION NCT03053141 RHythmia mAPping and Signal acquisitiOn for Data analYsis (RHAPSODY) RECRUITING NCT07274527 Amnioinfusion's Protective Effects on Respiratory and Longitudinal Pediatric Outcomes After Intrapartum Thick Meconium Exposure RECRUITING NCT07572253 A Study of Using CARTO SOUND™ FAM to Guide Pulsed Field Ablation for Atrial Fibrillation NOT_YET_RECRUITING NCT07576790 Evaluation of Balloon Guide Catheter as Proximal Protection During Carotid Artery Stenting (EMBO-PROTECT) NOT_YET_RECRUITING

Other Devices by Seigla Medical, Inc.

K243691LiquID .051 LP Guide Catheter Extension

Related Devices (Code: DQY)

K163000AMPLATZER TorqVue 45x45 Delivery SheathAga Medical COrporation (Wholly Owned by St. Jude Medical CO K160561Boosting CatheterQxmedical, LLC K161546R2P SlenGuideAshitaka Factory of Terumo Corporation K161152Navien Intracranial Support CatheterMicro Therapeutics, Inc. d/b/a ev3 Neurovascular K162384TrailBlazer Angled Support CatheterMedtronic Vascular, Inc.(Formerly Ev3 Inc.) K162359Surefire Guiding CatheterSurefire Medical, Inc.

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.

↑