510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K974883Substantially Equivalent

Bactec Mgit 960 System

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

K974883 is the FDA 510(k) clearance record for BACTEC MGIT 960 SYSTEM, a class I device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code MDB (System, Blood Culturing). FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show 2 recalls naming K974883.

Clearance record

Decision date
Received
(122 days to decision)
Product code
MDB System, Blood Culturing
Regulation
21 CFR 866.2560
Device class
Class I
Review panel
Microbiology
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic P.O. Box 243, Cockeysville MD
510(k) summary
Summary
Third party review
No

Clearances, product code MDB

Trailing 12 months
1 clearance under product code MDB in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MDB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260