Pft Filter

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K952062 ↗

FDA Product Code

CAH

Device Class

Class II

Regulation

21 CFR Part 868.5260

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K961318 Active Cleared 17 Dec 1996

• 1ST Response (Tm) Infant Manual Resuscitator

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• Intertech/Inspiron (R) Medication Nebulizer Kit

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  FDA 510(k) K896923 Active Cleared 12 Mar 1990

• Disposable Anesthesia Breathing Circuits, Modified

  Class I

  FDA 510(k) K912065 Active Cleared 23 Oct 1991

See all devices from Intertech Resources, Inc. →