Conductive Anesthsia Breath. Circuit

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

510(k) Number

K760149 ↗

FDA Product Code

CAI

Device Class

Class I

Regulation

21 CFR Part 868.5240

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Anesthesia Bacteria Filter

  Class II

  FDA 510(k) K820577 Active Cleared 18 Mar 1982

• Mainflow Bacteria Filter

  Class II

  FDA 510(k) K820576 Active Cleared 18 Mar 1982

• Disposable Bacteria Filter

  Class II

  FDA 510(k) K770136 Active Cleared 14 Feb 1977

• Emergency Tracheostomy Kit

  Class I

  FDA 510(k) K823872 Active Cleared 21 Jan 1983

• Protect IV Gard

  Class I

  FDA 510(k) K772060 Active Cleared 20 Dec 1977

• Airway, Berman 40, 60, 80, 90, L00MM'S

  Class I

  FDA 510(k) K770001 Active Cleared 12 Jan 1977

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