Nrt X-Ray A/S
Nrt X-Ray A/S holds FDA 510(k) medical device clearances, first cleared 2018, most recent 2024, with 4 FDA device recalls on record.
Top product codes for Nrt X-Ray A/S
FDA recalls by Nrt X-Ray A/S
- Z-1784-2024 — Intelli-C: Right side suspended Tabletop, REF: 03400000; Left side suspended Tabletop, REF: 03400010, used with the Intelli-C X-ray system
- Z-1669-2023 — Intelli-C, Left side suspended Tabletop, REF: 03400010
- Z-1668-2023 — Intelli-C, Right side suspended Tabletop, REF: 03400000
- Z-0526-2022 — 1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C devices)
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 Nrt X-Ray A/S
Data sourced from openFDA. This site is unofficial and independent of the FDA.