K-number	K812238
Device name	D.I.V.A.S.
Applicant	Cgr Medical Corp.
Product code	IZI
Device class	Class II
Decision date	Sep 11, 1981
Decision	Substantially Equivalent
Regulation	892.1600

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View the full FDA submission: accessdata.fda.gov

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D.I.V.A.S.

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