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FDA 510(k) Applications for Medical Device Product Code "CEL"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K905829 | KAMIYA BIOMEDICAL CO. | DETERMINER PL/DETERMINATION OF PHOSPHOLIPIDS | 01/30/1991 |
K884169 | THE DU PONT CO. | DU PONT ANALYST THYROID ROTOR | 01/24/1989 |
K801076 | WAKO PURE CHEMICAL INDUSTRIES, LTD. | WAKO PHOSPHOLIPIDS TEST | 06/30/1980 |