K-number	K791783
Device name	OMNI-STANICOR (THETA) MOD 237A
Applicant	Cordis Corp.
Product code	DXY
Device class	Class III
Decision date	Oct 22, 1979
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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OMNI-STANICOR (THETA) MOD 237A

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