510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901362Substantially Equivalent

Accessory Fitment to Nebulizer System, Sterile

Automatic Liquid Packaging, Inc., Woodstock IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901362 is the FDA 510(k) clearance record for ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE, a class II device, cleared for Automatic Liquid Packaging, Inc. on under FDA product code CAF (Nebulizer (Direct Patient Interface)). FDA records list 21 510(k) clearances for Automatic Liquid Packaging, Inc., from to . As of , FDA records show no recalls naming K901362.

Clearance record

Decision date
Received
(75 days to decision)
Product code
CAF Nebulizer (Direct Patient Interface)
Regulation
21 CFR 868.5630
Device class
Class II
Review panel
Anesthesiology
Applicant
Automatic Liquid Packaging, Inc. 2200 W. Lake Shore Dr., Woodstock IL
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