FDA 510(k) Applications for Medical Device Product Code "NGE"
(Test, Luteinizing Hormone (Lh), Over The Counter)

FDA 510(k) Number Applicant Device Name Decision Date
K973860 CONCEPTION TECHNOLOGY, INC. OVULON MONITOR 01/07/1998
K020808 PHEROMONE SCIENCES CORP. FERTILITE OV 09/23/2002
K981207 UNIPATH LTD. CLEARPLAN EASY FERTILITY MONITOR 10/28/1998
K990223 UNIPATH LTD. MODIFICATION OF CLEARPLAN EASY FERTILITY MONITOR 02/24/1999


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