K-number	K810392
Device name	OESOPHAGEAL THERAPY KIT
Applicant	Keymed, Inc.
Product code	KNT
Device class	Class II
Decision date	Mar 31, 1981
Decision	Substantially Equivalent
Regulation	876.5980

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View the full FDA submission: accessdata.fda.gov

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OESOPHAGEAL THERAPY KIT

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