Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K070691Substantially Equivalent

Bbl Chromagar 0157

Becton Dickinson & Co, Sparks MD / Traditional, Substantially Equivalent

K070691 is the FDA 510(k) clearance record for BBL CHROMAGAR 0157, a class I device, cleared for Becton, Dickinson & CO on under FDA product code JSI (Culture Media, Selective And Differential). FDA records list 345 510(k) clearances for Becton, Dickinson & CO, from to . As of , FDA records show no recalls naming K070691.

Clearance record

Decision date
Received
(252 days to decision)
Product code
JSI Culture Media, Selective And Differential
Regulation
21 CFR 866.2360
Device class
Class I
Review panel
Microbiology
Applicant
Becton, Dickinson & CO 7loveton Cir., Sparks MD
510(k) summary
Summary PDF
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