FDA 510(k) Applications for Medical Device Product Code "PZL"

FDA 510(k) Number Applicant Device Name Decision Date
DEN160037 SANUWAVE, INC. dermaPACE System 12/28/2017
K231710 Softwave./TRT LLC OW100S 09/01/2023
K202112 Storz Medical AG Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia Handpiece 02/21/2021
K191961 Tissue Regeneration Technologies OrthoGold 11/26/2019
K200926 Tissue Regeneration Technologies, LLC OrthoGold 100 08/28/2020


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