510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K832955Substantially Equivalent

Bacteroides Bile Esculin Agar

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

K832955 is the FDA 510(k) clearance record for BACTEROIDES BILE ESCULIN AGAR, a class I device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code JSI (Culture Media, Selective And Differential). FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show one recall naming K832955.

Clearance record

Decision date
Received
(29 days to decision)
Product code
JSI Culture Media, Selective And Differential
Regulation
21 CFR 866.2360
Device class
Class I
Review panel
Microbiology
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic 1875 Eye St. NW Suite 625, Washington DC
Third party review
No

Clearances, product code JSI

Trailing 12 months

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

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