FDA 510(k) Applications Submitted by KATHY LOWTHER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K980281 | 01/26/1998 | WELCH ALLYN XENON 300 LIGHT SOURCE | WELCH ALLYN, INC. |
| K981937 | 06/02/1998 | WELCH ALLYN REVEAL INTRAORAL CAMERA SYSTEM | WELCH ALLYN, INC. |
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