FDA 510(k) Applications Submitted by JOSEPH FALVO
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000566 | 02/22/2000 | MODOFICATION TO VITRO IMMUNODIAGNOSTIC PRODUCTS PSA REAGENT PACK, VITRO IMMUNODIAGNOSTIC PRODUCTS PSA CALIBRATORS | Ortho-Clinical Diagnostics, Inc. |
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