K-number	K843532
Device name	UROPAPER EIKEN 8
Applicant	Syn-Kit, Inc.
Product code	KHE
Device class	Class II
Decision date	Dec 12, 1984
Decision	Substantially Equivalent
Regulation	864.6550

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View the full FDA submission: accessdata.fda.gov

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UROPAPER EIKEN 8

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