510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K843835Substantially Equivalent

Ohmeda PEEP Valve for Gms Absorber

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

K843835 is the FDA 510(k) clearance record for OHMEDA PEEP VALVE FOR GMS ABSORBER, a class II device, cleared for Ohmeda Medical on under FDA product code BYE (Attachment, Breathing, Positive End Expiratory Pressure). FDA records list 888 510(k) clearances for GE HEALTHCARE, from to . As of , FDA records show no recalls naming K843835.

Clearance record

Decision date
Received
(45 days to decision)
Product code
BYE Attachment, Breathing, Positive End Expiratory Pressure
Regulation
21 CFR 868.5965
Device class
Class II
Review panel
Anesthesiology
Applicant
Ohmeda Medical P.O. Box 7550, Madison WI
Third party review
No

Clearances, product code BYE

Trailing 12 months

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

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