FDA 510(k) Applications Submitted by THE KENDALL COMPANY, L.P.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990530 | 02/19/1999 | KERLIX MD ANTIMICROBIAL GAUZE DRESSING | THE KENDALL COMPANY, L.P. |
| K992079 | 06/21/1999 | KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325 | THE KENDALL COMPANY, L.P. |
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