510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883560Substantially Equivalent

Cdt Cytotoxi Test

Advanced Clinical Diagnostics, Toledo OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883560 is the FDA 510(k) clearance record for CDT CYTOTOXI TEST, a class I device, cleared for Advanced Clinical Diagnostics on under FDA product code LLH (Reagents, Clostridium Difficile Toxin). FDA records list 19 510(k) clearances for Advanced Clinical Diagnostics, from to . As of , FDA records show no recalls naming K883560.

Clearance record

Decision date
Received
(67 days to decision)
Product code
LLH Reagents, Clostridium Difficile Toxin
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Advanced Clinical Diagnostics 3110 Drummond Rd., Toledo OH
Third party review
No

Clearances, product code LLH

Trailing 12 months

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

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