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FDA 510(k) Applications for Medical Device Product Code "JIH"
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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 |