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FDA 510(k)

TRANSIT-2 INFUSION CATHETER

K-Number: K950909 · 1995-05-16

ApplicantCordis Neurovascular, Inc.
Decision Date1995-05-16
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRANSIT-2 INFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Neurovascular, Inc.. It received FDA 510(k) clearance on 1995-05-16 under 510(k) number K950909. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSIT-2 INFUSION CATHETER?

TRANSIT-2 INFUSION CATHETER is a medical device that received FDA 510(k) clearance on 1995-05-16. The listed applicant is Cordis Neurovascular, Inc.. The 510(k) number is K950909.

When did TRANSIT-2 INFUSION CATHETER receive FDA 510(k) clearance?

TRANSIT-2 INFUSION CATHETER received FDA 510(k) clearance on 1995-05-16, under 510(k) number K950909.

Who is the listed applicant for TRANSIT-2 INFUSION CATHETER?

The FDA 510(k) record lists Cordis Neurovascular, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSIT-2 INFUSION CATHETER?

The FDA product code for TRANSIT-2 INFUSION CATHETER is DQO.

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Related Devices (Code: DQO)

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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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