FDA 510(k) Applications Submitted by CHARLES PENNINGTON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K071711 | 06/22/2007 | ASCA-CHEK | TECHLAB INC., CORPORATE RESEARCH CENTER |
| K071712 | 06/22/2007 | LEUKO EZ VUE | TECHLAB INC., CORPORATE RESEARCH CENTER |
| K082499 | 08/29/2008 | C. DIFF QUIK CHEK COMPLETE | TECHLAB, INC. |
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