FDA 510(k) Applications Submitted by SMITH HELMS MULLISS & MOORE, L.L.P.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K945590 | 11/14/1994 | SCOPETEX(TM) | SMITH HELMS MULLISS & MOORE, L.L.P. |
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