K-number	K810180
Device name	WILLIAMS OESOPHAGEAL VARICES INJECT TUBE
Applicant	Keymed, Inc.
Product code	FED
Device class	Class II
Decision date	Feb 9, 1981
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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WILLIAMS OESOPHAGEAL VARICES INJECT TUBE

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