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FDA 510(k)

PERCUPRO MESSENGER BALLOON CATHETER

K-Number: K094048 · 2011-07-14

ApplicantCardiosolutions, Inc.
Decision Date2011-07-14
Product CodeDYG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERCUPRO MESSENGER BALLOON CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cardiosolutions, Inc.. It received FDA 510(k) clearance on 2011-07-14 under 510(k) number K094048. The device is classified under product code DYG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUPRO MESSENGER BALLOON CATHETER?

PERCUPRO MESSENGER BALLOON CATHETER is a medical device that received FDA 510(k) clearance on 2011-07-14. The listed applicant is Cardiosolutions, Inc.. The 510(k) number is K094048.

When did PERCUPRO MESSENGER BALLOON CATHETER receive FDA 510(k) clearance?

PERCUPRO MESSENGER BALLOON CATHETER received FDA 510(k) clearance on 2011-07-14, under 510(k) number K094048.

Who is the listed applicant for PERCUPRO MESSENGER BALLOON CATHETER?

The FDA 510(k) record lists Cardiosolutions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERCUPRO MESSENGER BALLOON CATHETER?

The FDA product code for PERCUPRO MESSENGER BALLOON CATHETER is DYG.

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 Cardiosolutions, Inc. 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.

K131332CARDIOSOLUTIONS PERCU-PRO STEERABLE INTRODUCERK094062PERCU-PRO GUIDEWIRE

Related Devices (Code: DYG)

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.

K242451HemoSphere Alta Advanced Monitoring Platform (ALTAALL1/ALTCR1/ALTASR1); HemoSphere Alta- monitor pressure cable (HEMAPSC200);Acumen AFM cable- HemoSphere Alta monitor (HEMAFM100)Edwards LifesciencesK233983Swan-Ganz Pacing Probe and Catheters; Swan-Ganz Bipolar Pacing Catheter (D97120F5); Swan-Ganz Bipolar Pacing Catheter (D97130F5); Swan-Ganz Pacing Thermodilution TD Catheter (D200F7); Chandler Transluminal V-Pacing Probe (D98100)Edwards LifesciencesK233824Swan-Ganz catheterEdwards Lifesciences, LLCK231248Swan-Ganz Catheters, FloTrac sensors, ClearSight finger cuffs, HemoSphere Advanced Monitoring PlatformEdwards Lifesciencess, LLCK222117Swang-Ganz IQ pulmonary artery catheterEdwards Lifesiences, LLCK193466Swan-Ganz CathetersEdwards Lifesciences, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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