FDA 510(k) Applications Submitted by PERIMMUNE, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970302 | 01/27/1997 | APO-TEK LP(A) | PERIMMUNE, INC. |
| K970353 | 01/30/1997 | AURA TEK FDP | PERIMMUNE, INC. |
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