FDA 510(k) Applications Submitted by LORETTA MOONEY

FDA 510(k) Number Submission Date Device Name Applicant
K190662 03/15/2019 MRI Compatibility for Existing Straumann Dental Implant Systems Straumann USA LLC
K041212 05/10/2004 HOUVA 3 PHOTOTHERAPY SYSTEM NATIONAL BIOLOGICAL CORP.
K051660 06/22/2005 DENTRONIX DDS 7000 RAPID DRY HEAT STERILIZER STERILIZATION SYSTEM COLTENE/WHALEDENT INC.


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