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
K982043Substantially Equivalent

Breneb

Bremed Italia, S.r.l., Arnold MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K982043 is the FDA 510(k) clearance record for BRENEB, a class II device, cleared for Bremed Italia, S.R.L. on under FDA product code CAF (Nebulizer (Direct Patient Interface)). FDA records list 3 510(k) clearances for Bremed Italia, S.R.L., from to . As of , FDA records show no recalls naming K982043.

Clearance record

Decision date
Received
(152 days to decision)
Product code
CAF Nebulizer (Direct Patient Interface)
Regulation
21 CFR 868.5630
Device class
Class II
Review panel
Anesthesiology
Applicant
Bremed Italia, S.R.L. 1337 Rockwood Forest Dr., Arnold MO
510(k) summary
Statement
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