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FDA 510(k) Applications Submitted by RANNDY KELLOGG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K062263
08/04/2006
OMRON MICRO-AIR VIBRATING MESH NEBULIZER, MODEL NE-U22
OMRON HEALTHCARE, INC.
K063690
12/12/2006
COLIN PRESS MATE, MODEL BP S510
OMRON HEALTHCARE, INC.
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