Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K012332Substantially Equivalent

Jas Carbon Dioxide Liquid Reagent

JAS Diagnostics/Drew Scientific, Miami FL / Traditional, Substantially Equivalent

K012332 is the FDA 510(k) clearance record for JAS CARBON DIOXIDE LIQUID REAGENT, a class II device, cleared for Jas Diagnostics, Inc. on under FDA product code KHS (Enzymatic, Carbon-Dioxide). FDA records list 20 510(k) clearances for JAS Diagnostics/Drew Scientific, from to . As of , FDA records show no recalls naming K012332.

Clearance record

Decision date
Received
(45 days to decision)
Product code
KHS Enzymatic, Carbon-Dioxide
Regulation
21 CFR 862.1160
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Jas Diagnostics, Inc. 7220 NW 58th St., Miami FL
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