FDA 510(k) Applications Submitted by John Ray

FDA 510(k) Number Submission Date Device Name Applicant
K961375 04/09/1996 DIA SCREEN 10 WAY REAGENT STRIPS GENESIS LABS, INC.
K232233 07/27/2023 Invisalign System with Mandibular Advancement Featuring Occlusal Blocks Align Technology, Inc.


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