Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K892060Substantially Equivalent

Cyberlab High Volume Drug Testing System

Syva Co., Palo Alto CA / Traditional, Substantially Equivalent

K892060 is the FDA 510(k) clearance record for CYBERLAB HIGH VOLUME DRUG TESTING SYSTEM, a class I device, cleared for Syva Co. on under FDA product code JQP (Calculator/Data Processing Module, For Clinical Use). FDA records list 140 510(k) clearances for Syva Co., from to . As of , FDA records show no recalls naming K892060.

Clearance record

Decision date
Received
(134 days to decision)
Product code
JQP Calculator/Data Processing Module, For Clinical Use
Regulation
21 CFR 862.2100
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Syva Co. 900 Arastradero Rd., Palo Alto CA
Third party review
No

Clearances, product code JQP

Trailing 12 months

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

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