FDA 510(k) Applications Submitted by Deep Blue Medical Advances, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K230227 01/27/2023 T-Line Hernia Mesh Deep Blue Medical Advances, Inc.
K221556 05/31/2022 T-Line Hernia Mesh Deep Blue Medical Advances, Inc.
K193144 11/13/2019 T-Line Hernia Mesh Deep Blue Medical Advances, Inc.


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