T-Handle Adapter, U-Handle & L Handler Adapter

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K851215 ↗

FDA Product Code

CAM

Device Class

Class I

Regulation

21 CFR Part 868.6885

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Penox Lift Chair

  Class II

  FDA 510(k) K851218 Active Cleared 21 Jun 1985

• Penox High Flow Manifold

  Class II

  FDA 510(k) K853775 Active Cleared 29 Nov 1985

• Fill Hose Safety Adapter

  Class I

  FDA 510(k) K851219 Active Cleared 18 Jun 1985

• Portable Liquid Oxygen Unit (Modification)

  Class II

  FDA 510(k) K863978 Active Cleared 15 Dec 1986

• Modified Penox Lift Chair

  Class II

  FDA 510(k) K862654 Active Cleared 18 Jul 1986

• Penox Dual Flow Minifold

  Class I

  FDA 510(k) K851217 Active Cleared 18 Jun 1985

See all devices from Penox Technologies, Inc. →