FDA 510(k) Applications for Medical Device Product Code "GTJ"
(Antisera, All Groups, N. Meningitidis)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K952791 | BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC | DIRECTIGEN MENINGITIS COMBO TEST | 05/30/1996 |
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