FDA 510(k)

CORDIS POLYPROPYLENE BURR HOLE RESERVOIR

K-Number: K925810 · 1994-03-02

Decision Date1994-03-02

Product CodeJXG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CORDIS POLYPROPYLENE BURR HOLE RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1994-03-02 under 510(k) number K925810. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS POLYPROPYLENE BURR HOLE RESERVOIR?

CORDIS POLYPROPYLENE BURR HOLE RESERVOIR is a medical device that received FDA 510(k) clearance on 1994-03-02. The listed applicant is Cordis Corp.. The 510(k) number is K925810.

When did CORDIS POLYPROPYLENE BURR HOLE RESERVOIR receive FDA 510(k) clearance?

CORDIS POLYPROPYLENE BURR HOLE RESERVOIR received FDA 510(k) clearance on 1994-03-02, under 510(k) number K925810.

Who is the listed applicant for CORDIS POLYPROPYLENE BURR HOLE RESERVOIR?

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 POLYPROPYLENE BURR HOLE RESERVOIR?

The FDA product code for CORDIS POLYPROPYLENE BURR HOLE RESERVOIR is JXG.

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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.