K-number	K810482
Device name	SOMATOSENSORY STIMULATOR
Applicant	Amplaid USA, Inc.
Product code	GWF
Device class	Class II
Decision date	Apr 29, 1981
Decision	Substantially Equivalent
Regulation	882.1870

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View the full FDA submission: accessdata.fda.gov

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SOMATOSENSORY STIMULATOR

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