Surveyor I, Respiratory Computer System

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K801526 ↗

FDA Product Code

BZC

Device Class

Class II

Regulation

21 CFR Part 868.1880

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

• Devilbiss Model 8500D

  Class II

  FDA 510(k) K874041 Active Cleared 23 Dec 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

• Devilbiss Oxygen Enricher

  Class II

  FDA 510(k) K770157 Active Cleared 7 Feb 1977

See all devices from The Devilbiss Co. →