Codman Quick Shunt Kit, Cat. #82-6570

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K934196 ↗

FDA Product Code

GWG

Device Class

Class II

Regulation

21 CFR Part 882.1480

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K902257 Active Cleared 19 Jul 1990

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  Class II

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See all devices from Codman & Shurtleff, Inc. →