BK210584 - Genesis RapidWeld II STW, model GRW-430-02
510(k) Number: BK210584
Applicant: GenesisBPS, LLC
Device Name: Genesis RapidWeld II STW, model GRW-430-02
Decision Date: 7/15/2022
On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.
510(k) Number: BK210584
Applicant: GenesisBPS, LLC
Device Name: Genesis RapidWeld II STW, model GRW-430-02
Decision Date: 7/15/2022