← Back to catalogue

Servo-u Ventilator System 4.1, Servo-n Ventilator System 4.1, Servo-u MR Ventil…

FDA 510(k)EUDAMED

Class II (US FDA 510(k))

510(k) K201874

by Maquet Critical Care AB

Identifiers

510(k) Number
K201874 FDA 510(k)
FDA Product Code
CBK FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 868.5895 FDA 510(k)
Regulation Number
868.5895 FDA 510(k)
Advisory Committee
Anesthesiology FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Servo-u Ventilator System 4.1, Servo-n Ventilator System 4.1, Servo-u MR Ventil… by Maquet Critical Care AB — Class II — MDR, FDA_510K — listed in FDA 510(k)…

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

MDR

United States Active

FDA_510K

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA 510(k) K201874 24 fields · synced Oct 8, 2026
  • EUDAMED 1 fields · synced May 19, 2026