510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K052439Substantially Equivalent

Aeskulisa Glia a and Aeskulisa Glia G

Aesku Diagnostics, Miami FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K052439 is the FDA 510(k) clearance record for AESKULISA GLIA A AND AESKULISA GLIA G, a class II device, cleared for Aesku Diagnostics on under FDA product code MST (Antibodies, Gliadin). FDA records list 9 510(k) clearances for Aesku Diagnostics, from to . As of , FDA records show no recalls naming K052439.

Clearance record

Decision date
Received
(154 days to decision)
Product code
MST Antibodies, Gliadin
Regulation
21 CFR 866.5750
Device class
Class II
Review panel
Immunology
Applicant
Aesku Diagnostics 8880 NW 18th Ter., Miami FL
510(k) summary
Statement
Third party review
No

Clearances, product code MST

Trailing 12 months

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

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