FDA 510(k)

CORDIS STABILIZER PLUS XS

K-Number: K962932 · 1996-10-25

Decision Date1996-10-25

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORDIS STABILIZER PLUS XS is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1996-10-25 under 510(k) number K962932. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS STABILIZER PLUS XS?

CORDIS STABILIZER PLUS XS is a medical device that received FDA 510(k) clearance on 1996-10-25. The listed applicant is Cordis Corp.. The 510(k) number is K962932.

When did CORDIS STABILIZER PLUS XS receive FDA 510(k) clearance?

CORDIS STABILIZER PLUS XS received FDA 510(k) clearance on 1996-10-25, under 510(k) number K962932.

Who is the listed applicant for CORDIS STABILIZER PLUS XS?

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 STABILIZER PLUS XS?

The FDA product code for CORDIS STABILIZER PLUS XS is DQX.

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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.