Lichen, Bacterial in Line Breathing Filter

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

510(k) Number

K980662 ↗

FDA Product Code

CAH

Device Class

Class II

Regulation

21 CFR Part 868.5260

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Cliniflo Incentive Spirometer

  Class II

  FDA 510(k) K003146 Active Cleared 21 Nov 2000

• Stealth Pilot Kit/ Stealth Spacer/Face Mask Kit

  Class II

  FDA 510(k) K981167 Active Cleared 18 Jun 1998

• Roadrunner, Pep Therapy Device

  Class II

  FDA 510(k) K991561 Active Cleared 10 Nov 1999

• Boeing, Positive Airway Pressure (Pap) Therapy Device

  Class II

  FDA 510(k) K991300 Active Cleared 12 Jul 1999

• Trust

  Class II

  FDA 510(k) K040718 Active Cleared 2 Apr 2004

• Acapella

  Class II

  FDA 510(k) K002768 Active Cleared 5 Dec 2000

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