510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K172348Substantially Equivalent

AESKUSLIDES nDNA (Crithidia luciliae), AESKUSLIDES nDNA (Crithidia luciliae) Demo Kit, AESKUSLIDES nDNA (Crithidia luciliae) Bulk kit x5, AESKUSLIDES nDNA (Crithidia luciliae) Bulk kit x10

Aesku.Diagnostics GmbH & Co. KG, Wendeslheim, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K172348 is the FDA 510(k) clearance record for AESKUSLIDES nDNA (Crithidia luciliae), AESKUSLIDES nDNA (Crithidia luciliae) Demo Kit, AESKUSLIDES nDNA (Crithidia luciliae) Bulk kit x5, AESKUSLIDES nDNA (Crithidia luciliae) Bulk kit x10, a class II device, cleared for Aesku.Diagnostics GmbH & Co. KG on under FDA product code LSW (Anti-Dna Antibody, Antigen And Control). FDA records list 2 510(k) clearances for Aesku.Diagnostics GmbH & Co. KG, from to . As of , FDA records show no recalls naming K172348.

Clearance record

Decision date
Received
(197 days to decision)
Product code
LSW Anti-Dna Antibody, Antigen And Control
Regulation
21 CFR 866.5100
Device class
Class II
Review panel
Immunology
Applicant
Aesku.Diagnostics GmbH & Co. KG Mikro-Forum-Ring 2, Wendeslheim, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LSW

Trailing 12 months

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

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