510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K782013Substantially Equivalent

Gono-Cell

Abbott Medical, Abbott Park IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K782013 is the FDA 510(k) clearance record for GONO-CELL, a class I device, cleared for Abbott Laboratories on under FDA product code JSX (Kit, Identification, Neisseria Gonorrhoeae). FDA records list 1,478 510(k) clearances for Abbott Medical, from to . As of , FDA records show no recalls naming K782013.

Clearance record

Decision date
Received
(139 days to decision)
Product code
JSX Kit, Identification, Neisseria Gonorrhoeae
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Abbott Laboratories One Abbott Park Rd., Abbott Park IL
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