K-number	K951630
Device name	AURAFLEX PROGESTERONE 150TEST PACK
Applicant	Organon Teknika Corp.
Product code	JLS
Device class	Class I
Decision date	May 8, 1995
Decision	Substantially Equivalent
Regulation	862.1620

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View the full FDA submission: accessdata.fda.gov

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AURAFLEX PROGESTERONE 150TEST PACK

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