510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K033106Substantially Equivalent

Captia Hsv 2 Igg Type Specific Elisa Kit

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

K033106 is the FDA 510(k) clearance record for CAPTIA HSV 2 IGG TYPE SPECIFIC ELISA KIT, a class II device, cleared for Trinity Biotech USA on under FDA product code MYF (Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-2). FDA records list 25 510(k) clearances for Trinity Biotech USA, from to . As of , FDA records show no recalls naming K033106.

Clearance record

Decision date
Received
(287 days to decision)
Product code
MYF Enzyme Linked Immunosorbent Assay, Herpes Simplex Virus, Hsv-2
Regulation
21 CFR 866.3305
Device class
Class II
Review panel
Microbiology
Applicant
Trinity Biotech USA 2823 Girts Rd., Jamestown NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MYF

Trailing 12 months

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

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