FDA 510(k) Applications Submitted by LEON WORTHAM
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K060968 | 04/07/2006 | STASIS - I, II AND III; SERATHAN - A, B; INTRIN - EA, SI CALCIUM CHLORIDE 0.02M; FIBRINOGEN CONTROL-NORMAL, LOW | WORTHAM LABORATORIES INC |
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