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FDA 510(k)

HOLLOW MOTOR DRIVE UNIT

K-Number: K901601 · 1990-07-06

ApplicantDevices For Vascular Intervention, Inc.
Decision Date1990-07-06
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HOLLOW MOTOR DRIVE UNIT 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 1990-07-06 under 510(k) number K901601. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOLLOW MOTOR DRIVE UNIT?

HOLLOW MOTOR DRIVE UNIT is a medical device that received FDA 510(k) clearance on 1990-07-06. The listed applicant is Devices For Vascular Intervention, Inc.. The 510(k) number is K901601.

When did HOLLOW MOTOR DRIVE UNIT receive FDA 510(k) clearance?

HOLLOW MOTOR DRIVE UNIT received FDA 510(k) clearance on 1990-07-06, under 510(k) number K901601.

Who is the listed applicant for HOLLOW MOTOR DRIVE UNIT?

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 HOLLOW MOTOR DRIVE UNIT?

The FDA product code for HOLLOW MOTOR DRIVE UNIT is LIT.

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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 CONTROLLERK914422DEVICES FOR VASCU INTERVENT ROTAT HEMOSTAT VALVEK911678ROTATING HEMOSTATIC VALVEK910205LP-60 LOW PRESSURE INFLATION DEVICEK883933INTRODUCING CATHETER

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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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