K-number	K884851
Device name	BIOFEEDBACK DEVICE TG3, TG4
Applicant	Moe
Product code	HCC
Device class	Class II
Decision date	Feb 3, 1989
Decision	Substantially Equivalent
Regulation	882.5050

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View the full FDA submission: accessdata.fda.gov

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BIOFEEDBACK DEVICE TG3, TG4

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