510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K092736Substantially Equivalent

Euroimmun Anti-M2-3E Elisa (Igg)

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

K092736 is the FDA 510(k) clearance record for EUROIMMUN ANTI-M2-3E ELISA (IGG), a class II device, cleared for Euroimmun Us, Inc. on under FDA product code DBM (Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control). FDA records list 37 510(k) clearances for Euroimmun Us, Inc., from to . As of , FDA records show no recalls naming K092736.

Clearance record

Decision date
Received
(363 days to decision)
Product code
DBM Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control
Regulation
21 CFR 866.5090
Device class
Class II
Review panel
Immunology
Applicant
Euroimmun Us, Inc. 95 Washington St., Morristown NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DBM

Trailing 12 months

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

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