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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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