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)

CPS DIRECT MEDIGUIDE ENABLED OUTER CATHETER

K-Number: K120296 · 2012-05-11

ApplicantSt. Jude Medical, Cardiac Rhythm Management Divisi
Decision Date2012-05-11
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CPS DIRECT MEDIGUIDE ENABLED OUTER CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is St. Jude Medical, Cardiac Rhythm Management Divisi. It received FDA 510(k) clearance on 2012-05-11 under 510(k) number K120296. 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 CPS DIRECT MEDIGUIDE ENABLED OUTER CATHETER?

CPS DIRECT MEDIGUIDE ENABLED OUTER CATHETER is a medical device that received FDA 510(k) clearance on 2012-05-11. The listed applicant is St. Jude Medical, Cardiac Rhythm Management Divisi. The 510(k) number is K120296.

When did CPS DIRECT MEDIGUIDE ENABLED OUTER CATHETER receive FDA 510(k) clearance?

CPS DIRECT MEDIGUIDE ENABLED OUTER CATHETER received FDA 510(k) clearance on 2012-05-11, under 510(k) number K120296.

Who is the listed applicant for CPS DIRECT MEDIGUIDE ENABLED OUTER CATHETER?

The FDA 510(k) record lists St. Jude Medical, Cardiac Rhythm Management Divisi as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CPS DIRECT MEDIGUIDE ENABLED OUTER CATHETER?

The FDA product code for CPS DIRECT MEDIGUIDE ENABLED OUTER CATHETER is DQY.

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 St. Jude Medical, Cardiac Rhythm Management Divisi 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.

K122090SJM CONFIRM IMPLANTABLE CARDIAC MONITORK120298CPS EXCEL MEDIGUIDE ENABLED GUIDEWIREK111943AGILLS PF DELIVERY SYSTEMK103250CPS DIRECT SL II SLITTABLE OUTER CATHETERK093858PSA CABLE, MODELS 4160 AND 4161 AND PSA CABLE ADAPTER, MODEL 4053AK092075CPS DIRECT SL II SLITTABLE OUTER CATHETER, MODELS DS2C001, DS2C002, DS2C003, DS2C004, DS2C005

View all 10 devices →

Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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.

↑