FDA 510(k)

EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID

K-Number: K855058 · 1986-01-10

Decision Date1986-01-10

Product CodeJXG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1986-01-10 under 510(k) number K855058. 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 EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID?

EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID is a medical device that received FDA 510(k) clearance on 1986-01-10. The listed applicant is Cordis Corp.. The 510(k) number is K855058.

When did EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID receive FDA 510(k) clearance?

EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID received FDA 510(k) clearance on 1986-01-10, under 510(k) number K855058.

Who is the listed applicant for EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID?

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 EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID?

The FDA product code for EVDS, EVMDS, LDS & IVMCS CENTRAL NERVOUS SYS FLUID is JXG.

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Other records listing Cordis Corp. as applicant

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Related Devices (Code: 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.