K-number	K970587
Device name	AD-TECH SUBDURAL ELECTRODE
Applicant	Ad-Tech Medical Instrument Corp
Product code	GYC
Device class	Class II
Decision date	May 9, 1997
Decision	Substantially Equivalent
Regulation	882.1310

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View the full FDA submission: accessdata.fda.gov

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AD-TECH SUBDURAL ELECTRODE

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