510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K891124Substantially Equivalent

Non-Rebreathing Airway and Mask(s) Kits

Airway Products, Inc., Blue Springs MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K891124 is the FDA 510(k) clearance record for NON-REBREATHING AIRWAY AND MASK(S) KITS, a class II device, cleared for Airway Products, Inc. on under FDA product code CBP (Valve, Non-Rebreathing). FDA records list one 510(k) clearance for Airway Products, Inc. As of , FDA records show no recalls naming K891124.

Clearance record

Decision date
Received
(224 days to decision)
Product code
CBP Valve, Non-Rebreathing
Regulation
21 CFR 868.5870
Device class
Class II
Review panel
Anesthesiology
Applicant
Airway Products, Inc. 710 Main St. - Suite L, Blue Springs MO
Third party review
No

Clearances, product code CBP

Trailing 12 months

FDA records hold no clearances under product code CBP in the trailing twelve months.

FDA records show no clearances under product code CBP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CBP, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260