Liebel-Flarsheim Company, LLC
Liebel-Flarsheim Company, LLC holds FDA 510(k) medical device clearances, first cleared 2016, most recent 2020, with 3 FDA device recalls on record.
Top product codes for Liebel-Flarsheim Company, LLC
FDA recalls by Liebel-Flarsheim Company, LLC
- Z-1992-2021 — HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)
- Z-2834-2018 — Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedures requiring a beam of diagnostic quality radiation, primarily for urological applications such as functional x-ray diagnostics, endourology and minimal invasive urology/ surgery.
- Z-2833-2018 — Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedures requiring a beam of diagnostic quality radiation, primarily for urological applications such as functional x-ray diagnostics, endourology and minimal invasive urology/ surgery.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Liebel-Flarsheim Company, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.