Air Compressor

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K850795 ↗

FDA Product Code

BTI

Device Class

Class II

Regulation

21 CFR Part 868.6250

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Bear 7 Ventilator

  Class II

  FDA 510(k) K912619 Active Cleared 11 Jun 1992

• Bear Jet-150 Ventilator

  Class II

  FDA 510(k) K842688 Active Cleared 26 Jul 1984

• Tri-Service Omv Vaporizer

  Class II

  FDA 510(k) K864589 Active Cleared 5 Jun 1987

• VHS 820 Humidifier

  Class II

  FDA 510(k) K893034 Active Cleared 14 Jul 1989

• Bear Nvm-1

  Class II

  FDA 510(k) K872660 Active Cleared 12 Feb 1988

• VH820 Humidifier

  Class II

  FDA 510(k) K842340 Active Cleared 17 Jul 1984

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