Medical Device
Manufacturing
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K803024Substantially Equivalent

Cdc Anaerobe Laked Bl Agar W/paramomy.

BD Becton Dickinson Vacutainer Systems Preanalytic, Washington DC / Traditional, Substantially Equivalent

K803024 is the FDA 510(k) clearance record for CDC ANAEROBE LAKED BL AGAR W/PARAMOMY., a class I device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code JSJ (Culture Media, Selective And Non-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 K803024.

Clearance record

Decision date
Received
(26 days to decision)
Product code
JSJ Culture Media, Selective And Non-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 JSJ

Trailing 12 months

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

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