FDA 510(k)

STANDARD/PEDIATRIC CORDIS HYDROCEPHALUS VALVES

K-Number: K861377 · 1986-06-19

Decision Date1986-06-19

Product CodeJXG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

STANDARD/PEDIATRIC CORDIS HYDROCEPHALUS VALVES is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1986-06-19 under 510(k) number K861377. 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 STANDARD/PEDIATRIC CORDIS HYDROCEPHALUS VALVES?

STANDARD/PEDIATRIC CORDIS HYDROCEPHALUS VALVES is a medical device that received FDA 510(k) clearance on 1986-06-19. The listed applicant is Cordis Corp.. The 510(k) number is K861377.

When did STANDARD/PEDIATRIC CORDIS HYDROCEPHALUS VALVES receive FDA 510(k) clearance?

STANDARD/PEDIATRIC CORDIS HYDROCEPHALUS VALVES received FDA 510(k) clearance on 1986-06-19, under 510(k) number K861377.

Who is the listed applicant for STANDARD/PEDIATRIC CORDIS HYDROCEPHALUS VALVES?

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 STANDARD/PEDIATRIC CORDIS HYDROCEPHALUS VALVES?

The FDA product code for STANDARD/PEDIATRIC CORDIS HYDROCEPHALUS VALVES 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.