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FDA 510(k)

REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM

K-Number: K102418 · 2011-04-15

ApplicantReverse Medical Corporation
Decision Date2011-04-15
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REVERSE MEDICAL REPORT GUIDE CATHETER 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 2011-04-15 under 510(k) number K102418. 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 REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM?

REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM is a medical device that received FDA 510(k) clearance on 2011-04-15. The listed applicant is Reverse Medical Corporation. The 510(k) number is K102418.

When did REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM receive FDA 510(k) clearance?

REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM received FDA 510(k) clearance on 2011-04-15, under 510(k) number K102418.

Who is the listed applicant for REVERSE MEDICAL REPORT GUIDE CATHETER 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 REPORT GUIDE CATHETER SYSTEM?

The FDA product code for REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM is DQY.

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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 MICROCATHETERK123803REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEMK122684REVERSE MEDICAL MICROCATHETERK112262REFLEX BALLON GUIDE CATHETERK110055REVERSE MEDICAL REFLEX GUIDE CATHETER

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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.

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