FDA 510(k) Applications Submitted by SHERYL RUPPEL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970353 | 01/30/1997 | AURA TEK FDP | PERIMMUNE, INC. |
| K991074 | 03/31/1999 | BARTELS LEGIONELLA URINARY ANTIGEN ELISA TEST | INTRACEL CORP. |
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