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FDA 510(k)

DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE

K-Number: K914422 · 1991-12-18

ApplicantDevices For Vascular Intervention, Inc.
Decision Date1991-12-18
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Devices For Vascular Intervention, Inc.. It received FDA 510(k) clearance on 1991-12-18 under 510(k) number K914422. 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 DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE?

DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE is a medical device that received FDA 510(k) clearance on 1991-12-18. The listed applicant is Devices For Vascular Intervention, Inc.. The 510(k) number is K914422.

When did DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE receive FDA 510(k) clearance?

DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE received FDA 510(k) clearance on 1991-12-18, under 510(k) number K914422.

Who is the listed applicant for DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE?

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

What is the FDA product code for DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE?

The FDA product code for DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVE is DQY.

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Other records listing Devices For Vascular Intervention, 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.

K935929MICROTRACKK920707HOLLOW MOTOR DRIVE UNIT W/ TORQUE CONTROLLERK911678ROTATING HEMOSTATIC VALVEK910205LP-60 LOW PRESSURE INFLATION DEVICEK901601HOLLOW MOTOR DRIVE UNITK883933INTRODUCING 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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