Devilbiss Model 8500D

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K874041 ↗

FDA Product Code

CAF

Device Class

Class II

Regulation

21 CFR Part 868.5630

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• De Vo/44 Oxygen Concentrator #444

  Class II

  FDA 510(k) K830174 Active Cleared 17 Feb 1983

• Devo/MC44 Oxygen Concentrator

  Class II

  FDA 510(k) K872470 Active Cleared 3 Aug 1987

• Pulmo-Aide Model 5610D

  Class I

  FDA 510(k) K854520 Active Cleared 9 Dec 1985

• Devo/MC29 Oxygen Concentrator MC29D

  Class II

  FDA 510(k) K852209 Active Cleared 24 Jun 1985

• Surveyor I, Respiratory Computer System

  Class II

  FDA 510(k) K801526 Active Cleared 21 Jul 1980

• Devilbiss Oxygen Enricher

  Class II

  FDA 510(k) K770157 Active Cleared 7 Feb 1977

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