FDA 510(k)

CODMAN* EXTERNAL DRAINAGE SYSTEM II (EDS-II)

K-Number: K902257 · 1990-07-19

Decision Date1990-07-19

Product CodeJXG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CODMAN* EXTERNAL DRAINAGE SYSTEM II (EDS-II) 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 1990-07-19 under 510(k) number K902257. 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* EXTERNAL DRAINAGE SYSTEM II (EDS-II)?

CODMAN* EXTERNAL DRAINAGE SYSTEM II (EDS-II) is a medical device that received FDA 510(k) clearance on 1990-07-19. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K902257.

When did CODMAN* EXTERNAL DRAINAGE SYSTEM II (EDS-II) receive FDA 510(k) clearance?

CODMAN* EXTERNAL DRAINAGE SYSTEM II (EDS-II) received FDA 510(k) clearance on 1990-07-19, under 510(k) number K902257.

Who is the listed applicant for CODMAN* EXTERNAL DRAINAGE SYSTEM II (EDS-II)?

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* EXTERNAL DRAINAGE SYSTEM II (EDS-II)?

The FDA product code for CODMAN* EXTERNAL DRAINAGE SYSTEM II (EDS-II) is 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.