Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K760766Substantially Equivalent

Pre-Set 50/50 Nitrous Oxide/oxygen Mixer

Fraser Sweatman, Inc., Mchenry IL / Traditional, Substantially Equivalent

K760766 is the FDA 510(k) clearance record for PRE-SET 50/50 NITROUS OXIDE/OXYGEN MIXER, a class II device, cleared for Fraser Sweatman, Inc. on under FDA product code BZR (Mixer, Breathing Gases, Anesthesia Inhalation). FDA records list 6 510(k) clearances for Fraser Sweatman, Inc., from to . As of , FDA records show no recalls naming K760766.

Clearance record

Decision date
Received
(4 days to decision)
Product code
BZR Mixer, Breathing Gases, Anesthesia Inhalation
Regulation
21 CFR 868.5330
Device class
Class II
Review panel
Anesthesiology
Applicant
Fraser Sweatman, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code BZR

Trailing 12 months

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

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