Comppac 200HD; CS12 Power Supply (Aircraft/Vechile); PS11 Power Supply (Mains)

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

510(k) Number

K040090 ↗

FDA Product Code

BTL

Models / Variants

Comppac 200HD

CS12 Power Supply (Aircraft/Vechile)

PS11 Power Supply (Mains)

FDA applicant

Pneupac , Ltd.

Device Class

Class II

Regulation

21 CFR Part 868.5925

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Pneupac Test Set, PT.#500-A250

  Class II

  FDA 510(k) K792458 Active Cleared 5 Feb 1980

• Compressor

  Class II

  FDA 510(k) K792457 Active Cleared 5 Feb 1980

• Models 2R and 3R Pneupac Ventilator/Resuscitator

  Class II

  FDA 510(k) K862830 Active Cleared 15 Oct 1986

• Pneupac Oxygen Therapy Unit

  Class II

  FDA 510(k) K792453 Active Cleared 5 Feb 1980

• Parapac

  Class II

  FDA 510(k) K960515 Active Cleared 10 Oct 1996

• Babypac

  Class II

  FDA 510(k) K970158 Active Cleared 28 Apr 1998

See all devices from Pneupac, Ltd. →