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

FDA 510(k)

NC TREK RX CORONARY DILATATION CATHETER

K-Number: K110134 · 2011-02-11

ApplicantAbbott Vascular-Cardiac Therapies
Decision Date2011-02-11
Product CodeLOX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NC TREK RX CORONARY DILATATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Vascular-Cardiac Therapies. It received FDA 510(k) clearance on 2011-02-11 under 510(k) number K110134. The device is classified under product code LOX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NC TREK RX CORONARY DILATATION CATHETER?

NC TREK RX CORONARY DILATATION CATHETER is a medical device that received FDA 510(k) clearance on 2011-02-11. The listed applicant is Abbott Vascular-Cardiac Therapies. The 510(k) number is K110134.

When did NC TREK RX CORONARY DILATATION CATHETER receive FDA 510(k) clearance?

NC TREK RX CORONARY DILATATION CATHETER received FDA 510(k) clearance on 2011-02-11, under 510(k) number K110134.

Who is the listed applicant for NC TREK RX CORONARY DILATATION CATHETER?

The FDA 510(k) record lists Abbott Vascular-Cardiac Therapies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NC TREK RX CORONARY DILATATION CATHETER?

The FDA product code for NC TREK RX CORONARY DILATATION CATHETER is LOX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Abbott Vascular-Cardiac Therapies as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K112957HI-TORQUE POWERTURNK103101HI-TORQUE BALANCE MIDDLEWEIGHT ELITEK103110MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETERK103153VOYAGER NC CORONARY DILATATION CATHETER AND NC TREK RX CORONARY DILATATION CATHETERK101116HI-TORQUE PILOT 50 AND 150 GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, HI-TORQUE WHISPER LS AND MS GUIDE WIRE WITH

Related Devices (Code: LOX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261428NC Euphora Rapid Exchange Balloon Dilatation CatheterMedtronic IrelandK261759Euphora Rapid Exchange (RX) Balloon Dilatation CatheterMedtronic IrelandK252116Firefighter™ Pro PTCA Balloon CatheterShanghai MicroPort Medical (Group) Co., Ltd.K254022FLASH Flex™ Aorto-Ostial Angioplasty SystemVerge Medical, Inc.K252295RyureiTerumo CorporationK251970Sprinter Legend Rapid Exchange Balloon Dilatation CatheterMedtronic, Ireland

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.

↑