Adult Anesthesia Breathing Circuit

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K932707 ↗

FDA Product Code

CAI

Device Class

Class I

Regulation

21 CFR Part 868.5240

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Connectors and Airway Extensions

  Class I

  FDA 510(k) K931345 Active Cleared 23 Apr 1993

• Pmp, Ltd. Custom Anesthesia Circuits

  Class I

  FDA 510(k) K932490 Active Cleared 14 Jul 1993

• Precision Med Products Ltd Mapleson D Circuits

  Class I

  FDA 510(k) K932708 Active Cleared 23 Jul 1993

• Precision Med Products Ltd Hyperinflation System

  Class II

  FDA 510(k) K932709 Active Cleared 23 Jul 1993

• Precision Med Products Ltd. Ventilator Hose

  Class I

  FDA 510(k) K932706 Active Cleared 23 Jul 1993

• Precision Med Products, Ltd. Breathing Bags

  Class I

  FDA 510(k) K932496 Active Cleared 16 Jul 1993

See all devices from Precision Med Products, Ltd. →