510(k) K850342

WYLER SUBDURAL STRIP ELECTRODE by Ad-Tech Medical Instrument Corp — Product Code GYC

K850342 is an FDA 510(k) premarket notification submitted by Ad-Tech Medical Instrument Corp for the device "WYLER SUBDURAL STRIP ELECTRODE". The FDA issued a decision of SN on July 30, 1985. The device falls under product code GYC (Electrode, Cortical), a Class II device regulated under 21 CFR 882.1310. Ad-Tech Medical Instrument Corp has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
July 30, 1985
Date Received
January 28, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Cortical
Device Class
Class II
Regulation Number
882.1310
Review Panel
NE
Submission Type