510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K990132Substantially Equivalent

Datex-Ohmeda Anesthesia Vaporizer, Model D-Tec

GE Healthcare, Madison WI / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K990132 is the FDA 510(k) clearance record for DATEX-OHMEDA ANESTHESIA VAPORIZER, MODEL D-TEC, a class II device, cleared for Datex-Ohmeda, Inc. on under FDA product code CAD (Vaporizer, Anesthesia, Non-Heated). FDA records list 888 510(k) clearances for GE HEALTHCARE, from to . As of , FDA records show no recalls naming K990132.

Clearance record

Decision date
Received
(7 days to decision)
Product code
CAD Vaporizer, Anesthesia, Non-Heated
Regulation
21 CFR 868.5880
Device class
Class II
Review panel
Anesthesiology
Applicant
Datex-Ohmeda, Inc. P.O. Box 7550, Madison WI
510(k) summary
Summary
Third party review
No

Clearances, product code CAD

Trailing 12 months

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

FDA records show no clearances under product code CAD in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CAD, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260