FDA 510(k) Applications Submitted by PROGRESSIVE SURGICAL PRODUCTS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K982439 | 07/14/1998 | PROXIDERM, MODELS TN 460, TN 90 460, BK 460 | PROGRESSIVE SURGICAL PRODUCTS, INC. |
| K970439 | 02/05/1997 | PROXIDERM (D-460,D 90 460,D 180,460, PS 460) | PROGRESSIVE SURGICAL PRODUCTS, INC. |
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