Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K011878Substantially Equivalent

Emit (R) Tox Salicylic Assay, Model 7So19ul, Emit (R) Tox Salicylic Acid Calibrators, Model 7S109ul

Syva Co., Cupertino CA / Traditional, Substantially Equivalent

K011878 is the FDA 510(k) clearance record for EMIT (R) TOX SALICYLIC ASSAY, MODEL 7SO19UL, EMIT (R) TOX SALICYLIC ACID CALIBRATORS, MODEL 7S109UL, a class II device, cleared for Syva Co. on under FDA product code DKJ (Colorimetry, Salicylate). FDA records list 4 510(k) clearances for Syva Co., from to . As of , FDA records show no recalls naming K011878.

Clearance record

Decision date
Received
(59 days to decision)
Product code
DKJ Colorimetry, Salicylate
Regulation
21 CFR 862.3830
Device class
Class II
Review panel
Clinical Toxicology
Applicant
Syva Co. 20400 Mariani Ave., Cupertino CA
510(k) summary
Summary
Third party review
No

Clearances, product code DKJ

Trailing 12 months

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

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