Stimtech Sd Clinician 6090 #78-8055

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K844212 ↗

FDA Product Code

GZJ

Device Class

Class II

Regulation

21 CFR Part 882.5890

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

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• Orbit Galaxy G2 Microcoil Delivery System

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• Codman Isocool Bipolar Forceps

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See all devices from Codman & Shurtleff, Inc. →