Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K960793Substantially Equivalent

Synermed Enzymatic CO2 Reagent Kit

Synermed, Inc., Quebec, Canada, CA / Traditional, Substantially Equivalent

K960793 is the FDA 510(k) clearance record for SYNERMED ENZYMATIC CO2 REAGENT KIT, a class II device, cleared for Synermed, Inc. on under FDA product code KHS (Enzymatic, Carbon-Dioxide). FDA records list 45 510(k) clearances for Synermed, Inc., from to . As of , FDA records show no recalls naming K960793.

Clearance record

Decision date
Received
(13 days to decision)
Product code
KHS Enzymatic, Carbon-Dioxide
Regulation
21 CFR 862.1160
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Synermed, Inc. 1688 50th Ave.,, Quebec, Canada, CA
510(k) summary
Statement
Third party review
No

Clearances, product code KHS

Trailing 12 months

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

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