FDA 510(k) Applications Submitted by HYBRITECH, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K972666 | 07/16/1997 | TANDEM-MP OSTASE IMMUNOENZYMETRIC ASSAY | HYBRITECH, INC. |
| K961573 | 04/23/1996 | TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAY | HYBRITECH, INC. |
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