K-number	K900021
Device name	PERCU-SET(TM)
Applicant	E-Z-Em, Inc.
Product code	HIO
Device class	Class I
Decision date	Mar 29, 1990
Decision	Substantially Equivalent
Regulation	884.1550

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View the full FDA submission: accessdata.fda.gov

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PERCU-SET(TM)

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