Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K012065Substantially Equivalent

Wiener Lab. Creatinina Cinetica Aa

Wiener Laboratories Saic, Rosario, Santa Fe, AR / Traditional, Substantially Equivalent

K012065 is the FDA 510(k) clearance record for WIENER LAB. CREATININA CINETICA AA, a class II device, cleared for Wiener Laboratories Saic on under FDA product code JFY (Enzymatic Method, Creatinine). FDA records list 24 510(k) clearances for Wiener Laboratories Saic, from to . As of , FDA records show no recalls naming K012065.

Clearance record

Decision date
Received
(100 days to decision)
Product code
JFY Enzymatic Method, Creatinine
Regulation
21 CFR 862.1225
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Wiener Laboratories Saic 2944 Riobamba, Rosario, Santa Fe, AR
510(k) summary
Summary
Third party review
No

Clearances, product code JFY

Trailing 12 months
1 clearance under product code JFY in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JFY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260