K-number	K914777
Device name	SIGMA PROCEDURE NO. 333-UV
Applicant	Sigma Diagnostics, Inc.
Product code	DML
Device class	Class II
Decision date	Dec 27, 1991
Decision	Substantially Equivalent
Regulation	862.3040

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View the full FDA submission: accessdata.fda.gov

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SIGMA PROCEDURE NO. 333-UV

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