FDA 510(k) Applications for Medical Device Product Code "MOQ"
(Battery, Replacement, Rechargeable)

FDA 510(k) Number Applicant Device Name Decision Date
K980224 ALEXANDER MFG. CO. ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822 04/02/1998
K013133 NORDIX, INC. NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 11/13/2001
K081713 VIDACARE CORPORATION VERTEBRAL ACCESS SYSTEM BY VIDACARE 11/21/2008


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