510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K083050Substantially Equivalent

Evite Xl

Draeger Medical AG & Co. KG, Telford PA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K083050 is the FDA 510(k) clearance record for EVITE XL, a class II device, cleared for Draeger Medical AG & Co. KG on under FDA product code CBK (Ventilator, Continuous, Facility Use). FDA records list 10 510(k) clearances for Draeger Medical AG & Co. KG, from to . As of , FDA records show no recalls naming K083050.

Clearance record

Decision date
Received
(76 days to decision)
Product code
CBK Ventilator, Continuous, Facility Use
Regulation
21 CFR 868.5895
Device class
Class II
Review panel
Anesthesiology
Applicant
Draeger Medical AG & Co. KG 3135 Quarry Rd., Telford PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CBK

Trailing 12 months
4 clearances under product code CBK in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CBK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260