510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K023860Substantially Equivalent

Microalbumin Reagent Set and Calibrators

Horiba Instruments Incorporated, Lincoln Park MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K023860 is the FDA 510(k) clearance record for MICROALBUMIN REAGENT SET AND CALIBRATORS, a class II device, cleared for Pointe Scientific, Inc., on under FDA product code DDZ (Albumin, Fitc, Antigen, Antiserum, Control). FDA records list 89 510(k) clearances for HORIBA INSTRUMENTS INCORPORATED, from to . As of , FDA records show no recalls naming K023860.

Clearance record

Decision date
Received
(159 days to decision)
Product code
DDZ Albumin, Fitc, Antigen, Antiserum, Control
Regulation
21 CFR 866.5040
Device class
Class II
Review panel
Immunology
Applicant
Pointe Scientific, Inc., 1025 John A. Papalas Dr., Lincoln Park MI
510(k) summary
Statement
Third party review
No

Clearances, product code DDZ

Trailing 12 months

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

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