FDA 510(k)

INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS

K-Number: K924600 · 1992-12-10

Decision Date1992-12-10

Product CodeJXG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1992-12-10 under 510(k) number K924600. 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 INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS?

INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS is a medical device that received FDA 510(k) clearance on 1992-12-10. The listed applicant is Cordis Corp.. The 510(k) number is K924600.

When did INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS receive FDA 510(k) clearance?

INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS received FDA 510(k) clearance on 1992-12-10, under 510(k) number K924600.

Who is the listed applicant for INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS?

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 INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS?

The FDA product code for INTEGRAL DRAINAGE/VENTRICULAR/LUMBAR DRAINAGE SETS 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.