Draegerwerk AG & CO Kgaa
Draegerwerk AG & CO Kgaa holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2026, with 1 FDA device recall on record.
Top product codes for Draegerwerk AG & CO Kgaa
FDA recalls by Draegerwerk AG & CO Kgaa
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 Draegerwerk AG & CO Kgaa
- K253647 — Evita (V800); Evita (V600)
- K242769 — VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)
- K222822 — VentStar Helix dual heated (N) Plus (MP02650), VentStar Helix heated (N) Plus (MP02608)
- K222024 — Evita V800, Evita V600
- K222207 — Babylog VN800, Babylog VN600
- K221118 — CO2 Mainstream Sensor
- K162821 — Babyleo TN500
- K093633 — INFINITY ACUTE CARE SYSTEM WORKSTATION CRITICAL CARE
Data sourced from openFDA. This site is unofficial and independent of the FDA.