FDA 510(k) Applications Submitted by SafePath Medical, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K180701 03/16/2018 SafePath Suturing System SafePath Medical, Inc.
K222944 09/26/2022 SafePath Sulturing System-Silk Suture, SafePath Sulturing System Polyamide Suture (Nylon) SafePath Sulturing System- Polypropylene Suture SafePath Medical, Inc.


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