FDA 510(k) Applications for Medical Device Product Code "LYF"
(Pneumocystis Carinii)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K992252 | CHEMICON INTL., INC. | LIGHT DIAGNOSTICS PNEUMOCYSTIS CARINII DFA, MODEL 31965 | 08/10/1999 |
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