510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873359Substantially Equivalent

Airlife Volume Venti. Circuit W/clear Cap Ex Valve

American Pharmaseal Div. Ahsc, Valencia CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873359 is the FDA 510(k) clearance record for AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE, a class I device, cleared for American Pharmaseal Div. Ahsc on under FDA product code CAI (Circuit, Breathing (W Connector, Adaptor, Y Piece)). FDA records list 64 510(k) clearances for American Pharmaseal Div. Ahsc, from to . As of , FDA records show no recalls naming K873359.

Clearance record

Decision date
Received
(77 days to decision)
Product code
CAI Circuit, Breathing (W Connector, Adaptor, Y Piece)
Regulation
21 CFR 868.5240
Device class
Class I
Review panel
Anesthesiology
Applicant
American Pharmaseal Div. Ahsc 27200 N. Tourney Rd., Valencia CA
Third party review
No

Clearances, product code CAI

Trailing 12 months

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

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