510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K840211Substantially Equivalent

Fibri-Prest Automate Ha34

Wellcome Diagnostics, Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K840211 is the FDA 510(k) clearance record for FIBRI-PREST AUTOMATE HA34, a class II device, cleared for Wellcome Diagnostics on under FDA product code KQJ (System, Fibrinogen Determination). FDA records list 28 510(k) clearances for Wellcome Diagnostics, from to . As of , FDA records show one recall naming K840211.

Clearance record

Decision date
Received
(43 days to decision)
Product code
KQJ System, Fibrinogen Determination
Regulation
21 CFR 864.7340
Device class
Class II
Review panel
Hematology
Applicant
Wellcome Diagnostics 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code KQJ

Trailing 12 months

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

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