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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