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FDA 510(k)

RECRUIT MICROCATHETER

K-Number: K091563 · 2009-07-30

ApplicantReverse Medical Corporation
Decision Date2009-07-30
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RECRUIT MICROCATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Reverse Medical Corporation. It received FDA 510(k) clearance on 2009-07-30 under 510(k) number K091563. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECRUIT MICROCATHETER?

RECRUIT MICROCATHETER is a medical device that received FDA 510(k) clearance on 2009-07-30. The listed applicant is Reverse Medical Corporation. The 510(k) number is K091563.

When did RECRUIT MICROCATHETER receive FDA 510(k) clearance?

RECRUIT MICROCATHETER received FDA 510(k) clearance on 2009-07-30, under 510(k) number K091563.

Who is the listed applicant for RECRUIT MICROCATHETER?

The FDA 510(k) record lists Reverse Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RECRUIT MICROCATHETER?

The FDA product code for RECRUIT MICROCATHETER is MMX.

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 Reverse Medical Corporation 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.

K133282REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEMK130858REVERSE MEDICAL MICROCATHETERK123803REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEMK122684REVERSE MEDICAL MICROCATHETERK112262REFLEX BALLON GUIDE CATHETERK102418REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM

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Related Devices (Code: MMX)

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.

K242776LimFlow V-CeiverLimFlow, Inc.K241259Amplatz Goose Neck Snare KitMedtronic, Inc.K232443Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval KitArgon Medical Devices, Inc.K222254Gunther Tulip Vena Cava Filter Retrieval SetCook IncorporatedK222083LimFlow V-CeiverLimFlow, Inc.K212988ONO Retrieval DeviceOnocor Vascular, LLC

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.

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