510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K925329Substantially Equivalent

Culturette Brand Toxin Cd Test

BD Becton Dickinson Vacutainer Systems Preanalytic, Columbus NE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925329 is the FDA 510(k) clearance record for CULTURETTE BRAND TOXIN CD TEST, a class I device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code LLH (Reagents, Clostridium Difficile Toxin). FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show no recalls naming K925329.

Clearance record

Decision date
Received
(154 days to decision)
Product code
LLH Reagents, Clostridium Difficile Toxin
Regulation
21 CFR 866.2660
Device class
Class I
Review panel
Microbiology
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic P.O. Box 987, Columbus NE
510(k) summary
Statement
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 November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LLH, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260