FDA 510(k)

TRANSIT INFUSION CATHETER (NEUROVASCULAR USE)

K-Number: K936282 · 1994-07-18

Decision Date1994-07-18

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

TRANSIT INFUSION CATHETER (NEUROVASCULAR USE) 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 1994-07-18 under 510(k) number K936282. 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 INFUSION CATHETER (NEUROVASCULAR USE)?

TRANSIT INFUSION CATHETER (NEUROVASCULAR USE) is a medical device that received FDA 510(k) clearance on 1994-07-18. The listed applicant is Cordis Neurovascular, Inc.. The 510(k) number is K936282.

When did TRANSIT INFUSION CATHETER (NEUROVASCULAR USE) receive FDA 510(k) clearance?

TRANSIT INFUSION CATHETER (NEUROVASCULAR USE) received FDA 510(k) clearance on 1994-07-18, under 510(k) number K936282.

Who is the listed applicant for TRANSIT INFUSION CATHETER (NEUROVASCULAR USE)?

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 INFUSION CATHETER (NEUROVASCULAR USE)?

The FDA product code for TRANSIT INFUSION CATHETER (NEUROVASCULAR USE) is DQO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.