510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K153303Substantially Equivalent

EUROIMMUN Anti-West Nile Virus ELISA (IgG)

Euroimmun US Inc., Morris Plains NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K153303 is the FDA 510(k) clearance record for EUROIMMUN Anti-West Nile Virus ELISA (IgG), a class II device, cleared for Euroimmun Us, Inc. on under FDA product code NOP (Elisa, Antibody, West Nile Virus). FDA's definition for product code NOP reads: "The West Nile Virus ELISA is intended for the detection of IgG and IgM antibodies to West Nile Virus. Specimens may be serum or cerebral spinal fluid from symptomatic patients". FDA records list 37 510(k) clearances for Euroimmun Us, Inc., from to . As of , FDA records show no recalls naming K153303.

Clearance record

Decision date
Received
(268 days to decision)
Product code
NOP Elisa, Antibody, West Nile Virus
Regulation
21 CFR 866.3940
Device class
Class II
Review panel
Microbiology
Applicant
Euroimmun Us, Inc. 1100 The American Rd., Morris Plains NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NOP

Trailing 12 months

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

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