510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K951539Substantially Equivalent

Enterococcus Screening Medium

Becton Dickinson Microbiology Systems, Cockeysville MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K951539 is the FDA 510(k) clearance record for ENTEROCOCCUS SCREENING MEDIUM, a class II device, cleared for Becton Dickinson Microbiology Systems on under FDA product code JWY (Manual Antimicrobial Susceptibility Test Systems). FDA records list 33 510(k) clearances for Becton Dickinson Microbiology Systems, from to . As of , FDA records show 4 recalls naming K951539.

Clearance record

Decision date
Received
(71 days to decision)
Product code
JWY Manual Antimicrobial Susceptibility Test Systems
Regulation
21 CFR 866.1640
Device class
Class II
Review panel
Microbiology
Applicant
Becton Dickinson Microbiology Systems P.O. Box 243, Cockeysville MD
510(k) summary
Summary
Third party review
No

Clearances, product code JWY

Trailing 12 months
2 clearances under product code JWY in the twelve months to October 2026, April 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code JWY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20262
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260