Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K933149Substantially Equivalent

Instrument Detergent Concentrate

Nobelpharma USA, Inc., Chicago IL / Traditional, Substantially Equivalent

K933149 is the FDA 510(k) clearance record for INSTRUMENT DETERGENT CONCENTRATE, a class I device, cleared for Nobelpharma USA, Inc. on under FDA product code FLG (Cleaner, Ultrasonic, Medical Instrument). FDA records list 64 510(k) clearances for Nobelpharma USA, Inc., from to . As of , FDA records show no recalls naming K933149.

Clearance record

Decision date
Received
(232 days to decision)
Product code
FLG Cleaner, Ultrasonic, Medical Instrument
Regulation
21 CFR 880.6150
Device class
Class I
Review panel
General Hospital
Applicant
Nobelpharma USA, Inc. 5101 S. Keeler Ave., Chicago IL
510(k) summary
Summary
Third party review
No

Clearances, product code FLG

Trailing 12 months

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

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