510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K823131Substantially Equivalent

Koagulab 40-a Automated Coagulation Sys

Ortho Diagnostic Systems, Inc., Carpinteria CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823131 is the FDA 510(k) clearance record for KOAGULAB 40-A AUTOMATED COAGULATION SYS, a class II device, cleared for Ortho Diagnostic Systems, Inc. on under FDA product code KQG (Instrument, Coagulation). FDA records list 126 510(k) clearances for Ortho Diagnostic Systems, Inc., from to . As of , FDA records show no recalls naming K823131.

Clearance record

Decision date
Received
(45 days to decision)
Product code
KQG Instrument, Coagulation
Regulation
21 CFR 864.5400
Device class
Class II
Review panel
Hematology
Applicant
Ortho Diagnostic Systems, Inc. 125 Mark Ave., Carpinteria CA
Third party review
No

Clearances, product code KQG

Trailing 12 months

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

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