510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K232507Substantially Equivalent

Aerogen®Solo Nebulizer System

Aerogen Ltd., Dangan Galway, IE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K232507 is the FDA 510(k) clearance record for Aerogen®Solo Nebulizer System, a class II device, cleared for Aerogen, Ltd. on under FDA product code CAF (Nebulizer (Direct Patient Interface)). FDA records list 10 510(k) clearances for Aerogen, Ltd., from to . As of , FDA records show no recalls naming K232507.

Clearance record

Decision date
Received
(266 days to decision)
Product code
CAF Nebulizer (Direct Patient Interface)
Regulation
21 CFR 868.5630
Device class
Class II
Review panel
Anesthesiology
Applicant
Aerogen, Ltd. Galway Business Park, Dangan Galway, IE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CAF

Trailing 12 months
4 clearances under product code CAF in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CAF, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260