Servo Ventilator 900 C/D

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K871354 ↗

FDA Product Code

CBK

Device Class

Class II

Regulation

21 CFR Part 868.5895

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

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  Class II

  FDA 510(k) K861625 Active Cleared 2 May 1986

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  Class II

  FDA 510(k) K861707 Active Cleared 19 Jun 1986

• Siemens-Elema Pulse Generator 625

  Class III

  FDA 510(k) K801508 Active Cleared 16 Sep 1980

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  Class III

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  Class I

  FDA 510(k) K840326 Active Cleared 7 Jun 1984

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  Class II

  FDA 510(k) K832959 Active Cleared 14 Nov 1983

See all devices from Siemens Elema AB →