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FDA 510(k)

REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM

K-Number: K123803 · 2013-07-02

ApplicantReverse Medical Corporation
Decision Date2013-07-02
Product CodeKRD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM 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 2013-07-02 under 510(k) number K123803. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM?

REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM is a medical device that received FDA 510(k) clearance on 2013-07-02. The listed applicant is Reverse Medical Corporation. The 510(k) number is K123803.

When did REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM receive FDA 510(k) clearance?

REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM received FDA 510(k) clearance on 2013-07-02, under 510(k) number K123803.

Who is the listed applicant for REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM?

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 REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM?

The FDA product code for REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM is KRD.

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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 MICROCATHETERK122684REVERSE MEDICAL MICROCATHETERK112262REFLEX BALLON GUIDE CATHETERK102418REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEMK110055REVERSE MEDICAL REFLEX GUIDE CATHETER

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Related Devices (Code: KRD)

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.

K252812UniPearls® Embolic MicrospheresSuzhou Haowei Medical Technology Co., Ltd.K261488OBSIDIO Conformable EmbolicBoston Scientific CorporationK261866Concerto Versa™ Detachable CoilMedtronic, Inc.K260635HARBOR Occlusion DeviceNuvascular, Inc.K260508LOBO Vascular Occlusion SystemOkami Medical, Inc.K253511Concerto Versa™ Detachable CoilMedtronic, Inc.

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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