Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K923844Substantially Equivalent

Lyris 100/120 Laboratory Information System

Biovation, Inc., Hercules CA / Traditional, Substantially Equivalent

K923844 is the FDA 510(k) clearance record for LYRIS 100/120 LABORATORY INFORMATION SYSTEM, a class I device, cleared for Biovation, Inc. on under FDA product code JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use). FDA records list 11 510(k) clearances for Biovation, Inc., from to . As of , FDA records show no recalls naming K923844.

Clearance record

Decision date
Received
(133 days to decision)
Product code
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use
Regulation
21 CFR 862.2300
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Biovation, Inc. 875alfred Nobel Dr., Hercules CA
510(k) summary
Summary
Third party review
No

Clearances, product code JJQ

Trailing 12 months

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

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