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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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