FDA 510(k)

CORDIS STEADFAST MAGNETIC EXCHANGE SYSTEM

K-Number: K942939 · 1994-08-31

Decision Date1994-08-31

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORDIS STEADFAST MAGNETIC EXCHANGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1994-08-31 under 510(k) number K942939. 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 CORDIS STEADFAST MAGNETIC EXCHANGE SYSTEM?

CORDIS STEADFAST MAGNETIC EXCHANGE SYSTEM is a medical device that received FDA 510(k) clearance on 1994-08-31. The listed applicant is Cordis Corp.. The 510(k) number is K942939.

When did CORDIS STEADFAST MAGNETIC EXCHANGE SYSTEM receive FDA 510(k) clearance?

CORDIS STEADFAST MAGNETIC EXCHANGE SYSTEM received FDA 510(k) clearance on 1994-08-31, under 510(k) number K942939.

Who is the listed applicant for CORDIS STEADFAST MAGNETIC EXCHANGE SYSTEM?

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

What is the FDA product code for CORDIS STEADFAST MAGNETIC EXCHANGE SYSTEM?

The FDA product code for CORDIS STEADFAST MAGNETIC EXCHANGE SYSTEM 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.