510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913456Substantially Equivalent

Visi-Neisseria

Kev Connecticut Diagnostics, Inc., Danielson CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913456 is the FDA 510(k) clearance record for VISI-NEISSERIA, a class I device, cleared for Kev Connecticut Diagnostics, Inc. on under FDA product code JSX (Kit, Identification, Neisseria Gonorrhoeae). FDA records list 2 510(k) clearances for Kev Connecticut Diagnostics, Inc., from to . As of , FDA records show no recalls naming K913456.

Clearance record

Decision date
Received
(67 days to decision)
Product code
JSX Kit, Identification, Neisseria Gonorrhoeae
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Kev Connecticut Diagnostics, Inc. 36c Beatrice Ave., Danielson CT
510(k) summary
Summary
Third party review
No

Clearances, product code JSX

Trailing 12 months

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

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