FDA 510(k) Applications Submitted by KERR CORPORATION (DANBURY)
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K020091 | 01/10/2002 | OPTILUX 501 | KERR CORPORATION (DANBURY) |
| K051545 | 06/10/2005 | L.E. DEMETRON II | KERR CORPORATION (DANBURY) |
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