FDA 510(k) Applications for Medical Device Product Code "LAG"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K073078 | AMERICAN BIO MEDICA CORP. | RAPID TOX CUP | 05/30/2008 |
K990786 | PRINCETON BIOMEDITECH CORP. | ACCUSIGN DOA 10, ACCUSIGN DOA 10 PANEL, ACUSIGN MET/OPI/COC/THC/PCP/BZO/BAR/MTD/TCA/AMP, BIOSIGN DOA10, BIOSIGN MET/OPI/ | 03/26/1999 |
K983501 | PRINCETON BIOMEDITECH CORP. | ACCUSIGN DOA 10,ACCUSIGN DOA PANEL,ACCUSIGN MET/OPI/COC/THC/PCP/BZO/BAR/MTD/TCA/AMP,BIOSIGN DOA 10, BIOSIGN MET/OPI/COC/ | 12/18/1998 |
K062575 | PRINCETON BIOMEDITECH CORP. | MODIFICATION TO: ACCUSIGN RC DOA 10 (MET/OPI/COC/THC/PCP/BZO/BAR/MTD/TCA/AMP | 11/26/2007 |