510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K874678Substantially Equivalent

I.m.n. Latex

Biokit USA, Inc., Barcelona, Spain / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K874678 is the FDA 510(k) clearance record for I.M.N. LATEX, a class II device, cleared for Biokit USA, Inc. on under FDA product code KTN (System, Test, Infectious Mononucleosis). FDA records list 16 510(k) clearances for Biokit USA, Inc., from to . As of , FDA records show no recalls naming K874678.

Clearance record

Decision date
Received
(31 days to decision)
Product code
KTN System, Test, Infectious Mononucleosis
Regulation
21 CFR 866.5640
Device class
Class II
Review panel
Immunology
Applicant
Biokit USA, Inc. Corcega 603-605, Barcelona, Spain
Third party review
No

Clearances, product code KTN

Trailing 12 months

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

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