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)

Ventricular Catheter

K-Number: K200950 · 2020-05-08

ApplicantAesculap, Inc.
Decision Date2020-05-08
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Ventricular Catheter is a medical device manufactured by Aesculap, Inc.. It received FDA 510(k) clearance on 2020-05-08 under approval number K200950. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ventricular Catheter?

Ventricular Catheter is a medical device that received FDA 510(k) clearance on 2020-05-08. It is manufactured by Aesculap, Inc.. The 510(k) number is K200950.

When was Ventricular Catheter approved by the FDA?

Ventricular Catheter received FDA 510(k) clearance on 2020-05-08, under approval number K200950.

What company makes Ventricular Catheter?

Ventricular Catheter is manufactured by Aesculap, Inc..

What is the FDA product code for Ventricular Catheter?

The FDA product code for Ventricular Catheter is JXG.

Related Clinical Trials

NCT01254474 Evaluation of Depolarization and Repolarisation Activity During Cardiac Arrhythmia Using a Novel Monophasic Action Potential Catheter COMPLETED NCT03053141 RHythmia mAPping and Signal acquisitiOn for Data analYsis (RHAPSODY) RECRUITING NCT06253858 Ultrasound (US) Guided External Ventricular Catheter Placement RECRUITING NCT05225935 Computed Tomography-Guided Catheter Ablation for Ventricular Tachycardia COMPLETED NCT05591118 Pulmonary Embolism - Thrombus Removal With Catheter-Directed Therapy RECRUITING NCT07585968 Safety and Effectiveness of the Sphere-9™ Catheter and Affera™ Ablation System for the Treatment of Ventricular Tachycardia (Sphere VT) NOT_YET_RECRUITING

Other Devices by Aesculap, Inc.

K152960ELAN 4 Motor System K160393AdTec K151165Aesculap Dafilon Nonabsorbable Polyamide Surgical Suture K172850SterilContainer with PrimeLine Pro Lid K173271Aesculap Slim Clip Applier Forceps K171001Monosyn Quick Synthetic Absorbable Surgical Suture

View all 34 devices →

Related Devices (Code: JXG)

K162437Codman EDS3 CSF External Drainage SystemCodman & Shurtleff, Inc. K161605Smart External Drain (SED) SystemAqueduct Critical Care, Inc. K161992Horizontal-Vertical Lumbar Valve Systems, Spetzler Lumbar Peritoneal Shunt SystemsIntegra LifeSciences Corporation K152700StrataMR Valves and ShuntsMedtronic Neurosurgery K153041Bundled Neurological Shunts and Accessories Product Families Labeling Modification to Support MR Conditional LabelingIntegra LifeSciences Corporation K152897Integra DP Valve Systems (including Burr Hole Reservoirs and Stainless Steel Connectors), Gravity Compensating AccessoryIntegra LifeSciences Corporation

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.

↑