FDA 510(k) Applications Submitted by FLEXSITE DIAGNOSTICS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971919 | 05/23/1997 | EZCHEK/HBA BLOOD COLLECTION KIT | FLEXSITE DIAGNOSTICS, INC. |
| K001810 | 06/15/2000 | URISITE URINE COLLECTION KIT FOR MICROALBUMIN/CREATININE TESTING | FLEXSITE DIAGNOSTICS, INC. |
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