K-number	K993681
Device name	DIGITEC TWO STAGE COMPRESSION KIT
Applicant	Digitec Medical Service Corp.
Product code	IZH
Device class	Class II
Decision date	Dec 21, 1999
Decision	Substantially Equivalent
Regulation	892.1710

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View the full FDA submission: accessdata.fda.gov

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DIGITEC TWO STAGE COMPRESSION KIT

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