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)

SAT CenterFlow Molding Balloon Catheter (IN20-00313)

K-Number: K243184 · 2025-06-25

ApplicantStrait Access Technologies Holdings
Decision Date2025-06-25
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SAT CenterFlow Molding Balloon Catheter (IN20-00313) is a medical device manufactured by Strait Access Technologies Holdings. It received FDA 510(k) clearance on 2025-06-25 under approval number K243184. 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 SAT CenterFlow Molding Balloon Catheter (IN20-00313)?

SAT CenterFlow Molding Balloon Catheter (IN20-00313) is a medical device that received FDA 510(k) clearance on 2025-06-25. It is manufactured by Strait Access Technologies Holdings. The 510(k) number is K243184.

When was SAT CenterFlow Molding Balloon Catheter (IN20-00313) approved by the FDA?

SAT CenterFlow Molding Balloon Catheter (IN20-00313) received FDA 510(k) clearance on 2025-06-25, under approval number K243184.

What company makes SAT CenterFlow Molding Balloon Catheter (IN20-00313)?

SAT CenterFlow Molding Balloon Catheter (IN20-00313) is manufactured by Strait Access Technologies Holdings.

What is the FDA product code for SAT CenterFlow Molding Balloon Catheter (IN20-00313)?

The FDA product code for SAT CenterFlow Molding Balloon Catheter (IN20-00313) is DQY.

Related Clinical Trials

NCT04647253 A Clinical Trial to Assess the Agent Paclitaxel Coated PTCA Balloon Catheter for the Treatment of Subjects With In-Stent Restenosis (ISR) ACTIVE_NOT_RECRUITING NCT06492174 A Clinical Trial to Assess the Agent Paclitaxel Coated PTCA Balloon Catheter for the Treatment of Subjects With In-Stent Restenosis (ISR) - Long Lesion Cohort ACTIVE_NOT_RECRUITING NCT07214948 Open, Randomized Feasibility Trial on the Safety and Performance of the INGA Catheter for Labor Induction NOT_YET_RECRUITING NCT07414771 Safety and Usability of the Inga Catheter for Labor Induction (INGA-MDP) NOT_YET_RECRUITING NCT07587541 Low-VOLTage Area-Guided Catheter Ablation and SVC Isolation for Persistent Atrial Fibrillation Using a Balloon-in-Basket Pulsed Field Ablation Catheter NOT_YET_RECRUITING NCT07583706 A Single-center, Single-arm Study to Evaluate the Safety and Efficacy of Ultra-minimally Invasive Prostate Dilation in Treating Patients With Significant Obstructive Symptoms Caused by Benign Prostatic Hyperplasia RECRUITING

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.

↑