510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K791329Substantially Equivalent

Fluoromatic Analyzer and Autosampler

Bio-Rad, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K791329 is the FDA 510(k) clearance record for FLUOROMATIC ANALYZER AND AUTOSAMPLER, a class I device, cleared for Bio-Rad on under FDA product code KHO (Fluorometer, For Clinical Use). FDA records list 319 510(k) clearances for Bio-Rad, from to . As of , FDA records show no recalls naming K791329.

Clearance record

Decision date
Received
(12 days to decision)
Product code
KHO Fluorometer, For Clinical Use
Regulation
21 CFR 862.2560
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Bio-Rad 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KHO

Trailing 12 months

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

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