FDA 510(k) Applications Submitted by SMITH KLINE DIAGNOSTICS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960183 | 01/16/1996 | FLEXSURE HP,CONTROLS FOR FLEXSUREHP,FLEXPACK HP(ABBOTT DIAGNOSTICS)ANDCONTROLS FOR FLEXPACK HP (ABBOTT DIAGNOSTICS) | SMITH KLINE DIAGNOSTICS, INC. |
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