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)

Stingray LP Catheter

K-Number: K231176 · 2023-05-25

ApplicantBoston Scientific
Decision Date2023-05-25
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Stingray LP Catheter is a medical device manufactured by Boston Scientific. It received FDA 510(k) clearance on 2023-05-25 under approval number K231176. 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 Stingray LP Catheter?

Stingray LP Catheter is a medical device that received FDA 510(k) clearance on 2023-05-25. It is manufactured by Boston Scientific. The 510(k) number is K231176.

When was Stingray LP Catheter approved by the FDA?

Stingray LP Catheter received FDA 510(k) clearance on 2023-05-25, under approval number K231176.

What company makes Stingray LP Catheter?

Stingray LP Catheter is manufactured by Boston Scientific.

What is the FDA product code for Stingray LP Catheter?

The FDA product code for Stingray LP Catheter is DQY.

Related Clinical Trials

NCT06170606 POLARx Post Approval Study (POLARx PAS) ACTIVE_NOT_RECRUITING NCT05501873 Real World Data Collection in Subjects Treated With the FARAPULSE Pulsed Field Ablation System ACTIVE_NOT_RECRUITING NCT04674969 Drug-Eluting Registry: Real-World Treatment of Lesions in the Peripheral Vasculature RECRUITING NCT04200937 IT Matters: The Erectile Restoration Registry ENROLLING_BY_INVITATION NCT06982235 Stone and Laser Therapies Post-Market Study (SALT) RECRUITING NCT01719055 RELIEF - A Global Prospective Observational Post-Market Study to Evaluate Long-Term Effectiveness of Neurostimulation Therapy for Pain RECRUITING

Other Devices by Boston Scientific

K160751Symphion Endoscope and Symphion Cervical Sheath DEN150040WallFlex Biliary RX Fully Covered Stent System RMV K173184Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle K163058Expect Slimline (SL) Endoscopic Ultrasound Aspiration Needle K180068ORISE Gel K180864WATCHMAN TruSeal Access System

View all 43 devices →

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.

↑