510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923903Substantially Equivalent

Vitek Immunodiagnostic Assay System Mumps Igg Assa

Biomerieux Vitek, Inc., Hazelwood MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923903 is the FDA 510(k) clearance record for VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM MUMPS IGG ASSA, a class I device, cleared for Biomerieux Vitek, Inc. on under FDA product code LJY (Enzyme Linked Immunoabsorbent Assay, Mumps Virus). FDA records list 49 510(k) clearances for Biomerieux Vitek, Inc., from to . As of , FDA records show no recalls naming K923903.

Clearance record

Decision date
Received
(370 days to decision)
Product code
LJY Enzyme Linked Immunoabsorbent Assay, Mumps Virus
Regulation
21 CFR 866.3380
Device class
Class I
Review panel
Microbiology
Applicant
Biomerieux Vitek, Inc. 595 Anglum Dr., Hazelwood MO
510(k) summary
Summary
Third party review
No

Clearances, product code LJY

Trailing 12 months

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

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