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
K925988Substantially Equivalent

Multifibren

Behring Diagnostics, Inc., Somerville NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925988 is the FDA 510(k) clearance record for MULTIFIBREN, a class II device, cleared for Behring Diagnostics, Inc. on under FDA product code KQJ (System, Fibrinogen Determination). FDA records list 145 510(k) clearances for Behring Diagnostics, Inc., from to . As of , FDA records show no recalls naming K925988.

Clearance record

Decision date
Received
(96 days to decision)
Product code
KQJ System, Fibrinogen Determination
Regulation
21 CFR 864.7340
Device class
Class II
Review panel
Hematology
Applicant
Behring Diagnostics, Inc. 17 Chubb Way, Somerville NJ
510(k) summary
Summary
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