510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K222822Substantially Equivalent

VentStar Helix dual heated (N) Plus (MP02650), VentStar Helix heated (N) Plus (MP02608)

Draegerwerk AG & Co. KGaA, Luebeck, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K222822 is the FDA 510(k) clearance record for VentStar Helix dual heated (N) Plus (MP02650), VentStar Helix heated (N) Plus (MP02608), a class II device, cleared for Draegerwerk AG & CO Kgaa on under FDA product code BZE (Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer). FDA records list 8 510(k) clearances for Draegerwerk AG & CO Kgaa, from to . As of , FDA records show no recalls naming K222822.

Clearance record

Decision date
Received
(268 days to decision)
Product code
BZE Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer
Regulation
21 CFR 868.5270
Device class
Class II
Review panel
Anesthesiology
Applicant
Draegerwerk AG & CO Kgaa Moislinger Allee 53-55, Luebeck, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BZE

Trailing 12 months
2 clearances under product code BZE in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code BZE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260