K-number	K955250
Device name	QI GONG MASSAGER
Applicant	East Health Development Group, Inc.
Product code	IRO
Device class	Class I
Decision date	Feb 8, 1996
Decision	Substantially Equivalent for Some Indications
Regulation	890.5975

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View the full FDA submission: accessdata.fda.gov

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QI GONG MASSAGER

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