FDA 510(k) Applications for Medical Device Product Code "JIH"
(Flame Photometry, Lithium)

FDA 510(k) Number Applicant Device Name Decision Date
K050338 Akers Biosciences, Inc. MODIFICATION TO: INSTAREAD LITHIUM SYSTEM 03/04/2005
K031579 AKERS LABORATORIES, INC. INSTAREAD LITHIUM SYSTEM 12/19/2003
K011033 DADE BEHRING, INC. DIMENSION LITHIUM (LI) FLEX REAGENT CARTRIDGE, MODEL DF 132 06/07/2001


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