510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K041974Substantially Equivalent

Med2000 Nebulizer Compressor, Models P3, P4, P5 with Nebulizer

Med2000 S.r.l., Great Neck NY / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K041974 is the FDA 510(k) clearance record for MED2000 NEBULIZER COMPRESSOR, MODELS P3, P4, P5 WITH NEBULIZER, a class II device, cleared for Med2000 S.R.L. on under FDA product code BTI (Compressor, Air, Portable). FDA records list 3 510(k) clearances for Med2000 S.R.L., from to . As of , FDA records show no recalls naming K041974.

Clearance record

Decision date
Received
(33 days to decision)
Product code
BTI Compressor, Air, Portable
Regulation
21 CFR 868.6250
Device class
Class II
Review panel
Anesthesiology
Applicant
Med2000 S.R.L. 55 Northern Blvd., Suite 200, Great Neck NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BTI

Trailing 12 months

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

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