510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K033079Substantially Equivalent

Chlamydia Igg Elisa Test System

Trinity Biotech USA, Jamestown NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K033079 is the FDA 510(k) clearance record for CHLAMYDIA IGG ELISA TEST SYSTEM, a class I device, cleared for Trinity Biotech USA on under FDA product code LJC (Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)). FDA records list 25 510(k) clearances for Trinity Biotech USA, from to . As of , FDA records show no recalls naming K033079.

Clearance record

Decision date
Received
(58 days to decision)
Product code
LJC Enzyme Linked Immunoabsorbent Assay, (Chlamydiae Group)
Regulation
21 CFR 866.3120
Device class
Class I
Review panel
Microbiology
Applicant
Trinity Biotech USA P.O. Box 1059, Jamestown NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LJC

Trailing 12 months

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

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