FDA 510(k)

CODMAN MICROSENSOR VENTRICULAR CATHETER KIT

K-Number: K991222 · 1999-07-09

ApplicantJohnson & Johnson Professionals, Inc.

Decision Date1999-07-09

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CODMAN MICROSENSOR VENTRICULAR CATHETER KIT 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 1999-07-09 under 510(k) number K991222. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODMAN MICROSENSOR VENTRICULAR CATHETER KIT?

CODMAN MICROSENSOR VENTRICULAR CATHETER KIT is a medical device that received FDA 510(k) clearance on 1999-07-09. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K991222.

When did CODMAN MICROSENSOR VENTRICULAR CATHETER KIT receive FDA 510(k) clearance?

CODMAN MICROSENSOR VENTRICULAR CATHETER KIT received FDA 510(k) clearance on 1999-07-09, under 510(k) number K991222.

Who is the listed applicant for CODMAN MICROSENSOR VENTRICULAR CATHETER KIT?

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 MICROSENSOR VENTRICULAR CATHETER KIT?

The FDA product code for CODMAN MICROSENSOR VENTRICULAR CATHETER KIT is GWM.

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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.