510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K990624Substantially Equivalent

Autostat II Anti-Sm/rnp Elisa

Cogent Diagnotics, Ltd., Midlothian, Scotland, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K990624 is the FDA 510(k) clearance record for AUTOSTAT II ANTI-SM/RNP ELISA, a class II device, cleared for Cogent Diagnotics , Ltd. on under FDA product code LKO (Anti-Rnp Antibody, Antigen And Control). FDA records list 31 510(k) clearances for Cogent Diagnotics , Ltd., from to . As of , FDA records show no recalls naming K990624.

Clearance record

Decision date
Received
(62 days to decision)
Product code
LKO Anti-Rnp Antibody, Antigen And Control
Regulation
21 CFR 866.5100
Device class
Class II
Review panel
Immunology
Applicant
Cogent Diagnotics , Ltd. Pentlands Science Park, Midlothian, Scotland, GB
510(k) summary
Statement
Third party review
No

Clearances, product code LKO

Trailing 12 months

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

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