510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K834570Substantially Equivalent

Volume Ventilator Circuit W/water Trap

Airlife, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K834570 is the FDA 510(k) clearance record for VOLUME VENTILATOR CIRCUIT W/WATER TRAP, a class I device, cleared for Airlife, Inc. on under FDA product code BZO (Set, Tubing And Support, Ventilator (W Harness)). FDA records list 76 510(k) clearances for Airlife, Inc., from to . As of , FDA records show no recalls naming K834570.

Clearance record

Decision date
Received
(67 days to decision)
Product code
BZO Set, Tubing And Support, Ventilator (W Harness)
Regulation
21 CFR 868.5975
Device class
Class I
Review panel
Anesthesiology
Applicant
Airlife, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code BZO

Trailing 12 months

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

FDA records show no clearances under product code BZO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BZO, 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