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FDA 510(k)

CODMAN-MEDOS VALVE SHUNT SYSTEM

K-Number: K944222 · 1995-07-28

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1995-07-28
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CODMAN-MEDOS VALVE SHUNT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1995-07-28 under 510(k) number K944222. 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 CODMAN-MEDOS VALVE SHUNT SYSTEM?

CODMAN-MEDOS VALVE SHUNT SYSTEM is a medical device that received FDA 510(k) clearance on 1995-07-28. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K944222.

When did CODMAN-MEDOS VALVE SHUNT SYSTEM receive FDA 510(k) clearance?

CODMAN-MEDOS VALVE SHUNT SYSTEM received FDA 510(k) clearance on 1995-07-28, under 510(k) number K944222.

Who is the listed applicant for CODMAN-MEDOS VALVE SHUNT SYSTEM?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CODMAN-MEDOS VALVE SHUNT SYSTEM?

The FDA product code for CODMAN-MEDOS VALVE SHUNT SYSTEM is JXG.

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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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