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FDA 510(k)

CORDIS HORIZONTAL-VERICAL VALVE SYSTEM

K-Number: K944595 · 1995-10-19

ApplicantCordis Corp.
Decision Date1995-10-19
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CORDIS HORIZONTAL-VERICAL VALVE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1995-10-19 under 510(k) number K944595. 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 HORIZONTAL-VERICAL VALVE SYSTEM?

CORDIS HORIZONTAL-VERICAL VALVE SYSTEM is a medical device that received FDA 510(k) clearance on 1995-10-19. The listed applicant is Cordis Corp.. The 510(k) number is K944595.

When did CORDIS HORIZONTAL-VERICAL VALVE SYSTEM receive FDA 510(k) clearance?

CORDIS HORIZONTAL-VERICAL VALVE SYSTEM received FDA 510(k) clearance on 1995-10-19, under 510(k) number K944595.

Who is the listed applicant for CORDIS HORIZONTAL-VERICAL VALVE SYSTEM?

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 HORIZONTAL-VERICAL VALVE SYSTEM?

The FDA product code for CORDIS HORIZONTAL-VERICAL VALVE SYSTEM 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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