FDA 510(k) Applications Submitted by HEMATRONIX, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960005 | 01/02/1996 | TRI-COURT 20-T | HEMATRONIX, INC. |
| K960471 | 02/01/1996 | TRI-COUNT 20 | HEMATRONIX, INC. |
| K972710 | 07/21/1997 | QUANTIFY(901) | HEMATRONIX, INC. |
| K993496 | 10/15/1999 | RETIC-QUINOX | HEMATRONIX, INC. |
| K012243 | 07/17/2001 | MCC URICHECK ASSAYED LIQUID URINE MULTICONSTITUENT CONTROL | HEMATRONIX, INC. |
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