K-number	K910683
Device name	ENZYMUN-TEST PROGESTERONE
Applicant	Boehringer Mannheim Corp.
Product code	JLS
Device class	Class I
Decision date	Apr 8, 1991
Decision	Substantially Equivalent
Regulation	862.1620

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View the full FDA submission: accessdata.fda.gov

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ENZYMUN-TEST PROGESTERONE

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