FDA 510(k) Applications Submitted by Rebound Therapeutics

FDA 510(k) Number Submission Date Device Name Applicant
K190075 01/16/2019 Aurora Evacuator Rebound Therapeutics
K180372 02/12/2018 Aurora Evacuator Rebound Therapeutics
K201637 06/16/2020 Aurora Evacuator +Coag Rebound Therapeutics
K201840 07/02/2020 Aurora Surgiscope System (Surgiscope), Aurora Surgiscope System (Image Control Box) Rebound Therapeutics
K191861 07/11/2019 Aurora Surgiscope System Rebound Therapeutics
K203745 12/22/2020 AURORA Evacuator +Coag Rebound Therapeutics


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