Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K013698Substantially Equivalent

Ast (Sgot)

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

K013698 is the FDA 510(k) clearance record for AST (SGOT), a class II device, cleared for Jas Diagnostics, Inc. on under FDA product code CIT (Nadh Oxidation/Nad Reduction, Ast/Sgot). FDA records list 20 510(k) clearances for JAS Diagnostics/Drew Scientific, from to . As of , FDA records show no recalls naming K013698.

Clearance record

Decision date
Received
(44 days to decision)
Product code
CIT Nadh Oxidation/Nad Reduction, Ast/Sgot
Regulation
21 CFR 862.1100
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 CIT

Trailing 12 months

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

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