FDA 510(k) Applications Submitted by ECTON, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K991872 | 06/01/1999 | LYNX ULTRASOUND SYSTEM | ECTON, INC. |
| K982800 | 08/10/1998 | ECTON LYNX ULTRASOUND SYSTEM | ECTON, INC. |
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