K-number	K800922
Device name	NORDICLAB PROGESTERONE RIA TEST
Applicant	Nordiclab Intl.
Product code	JLS
Device class	Class I
Decision date	May 14, 1980
Decision	Substantially Equivalent
Regulation	862.1620

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View the full FDA submission: accessdata.fda.gov

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NORDICLAB PROGESTERONE RIA TEST

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