FDA 510(k)

CODMAN BACTISEAL ENDOSCOPIC VENTICULAR CATHETER

K-Number: K110751 · 2011-05-09

Decision Date2011-05-09

Product CodeJXG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CODMAN BACTISEAL ENDOSCOPIC VENTICULAR CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 2011-05-09 under 510(k) number K110751. 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 BACTISEAL ENDOSCOPIC VENTICULAR CATHETER?

CODMAN BACTISEAL ENDOSCOPIC VENTICULAR CATHETER is a medical device that received FDA 510(k) clearance on 2011-05-09. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K110751.

When did CODMAN BACTISEAL ENDOSCOPIC VENTICULAR CATHETER receive FDA 510(k) clearance?

CODMAN BACTISEAL ENDOSCOPIC VENTICULAR CATHETER received FDA 510(k) clearance on 2011-05-09, under 510(k) number K110751.

Who is the listed applicant for CODMAN BACTISEAL ENDOSCOPIC VENTICULAR CATHETER?

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

What is the FDA product code for CODMAN BACTISEAL ENDOSCOPIC VENTICULAR CATHETER?

The FDA product code for CODMAN BACTISEAL ENDOSCOPIC VENTICULAR CATHETER is JXG.

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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.