510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K823520Substantially Equivalent

Fibrosystem

BD Becton Dickinson Vacutainer Systems Preanalytic, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823520 is the FDA 510(k) clearance record for FIBROSYSTEM, a class I device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code GKQ (Test, Thromboplastin Generation). FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show no recalls naming K823520.

Clearance record

Decision date
Received
(29 days to decision)
Product code
GKQ Test, Thromboplastin Generation
Regulation
21 CFR 864.7900
Device class
Class I
Review panel
Hematology
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic 1875 Eye St. NW Suite 625, Washington DC
Third party review
No

Clearances, product code GKQ

Trailing 12 months

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

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