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
K024217Substantially Equivalent

Liquichek Ana Control, Speckled Pattern, Positive, Catalog #108

Bio-Rad, Irvine CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K024217 is the FDA 510(k) clearance record for LIQUICHEK ANA CONTROL, SPECKLED PATTERN, POSITIVE, CATALOG #108, a class II device, cleared for Bio-Rad on under FDA product code DHN (Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control). FDA records list 319 510(k) clearances for Bio-Rad, from to . As of , FDA records show no recalls naming K024217.

Clearance record

Decision date
Received
(23 days to decision)
Product code
DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
Regulation
21 CFR 866.5100
Device class
Class II
Review panel
Immunology
Applicant
Bio-Rad 9500 Jeronimo Rd., Irvine CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DHN

Trailing 12 months

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

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