BD BACTEC PLUS ANAEROBIC/F (PLASTIC)— 510(k) K141810

Substantially Equivalent

Becton, Dickinson and Company

FDA 510(k) clearance K141810 for BD BACTEC PLUS ANAEROBIC/F (PLASTIC), Substantially Equivalent on 2014-12-10. Applicant: Becton, Dickinson and Company.

Clearance details

Applicant: Becton, Dickinson and Company
Product code: Code MDB
Advisory panel: Microbiology
Date received: 2014-07-07
Decision date: 2014-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sparks, MD, US

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Adverse events under product code MDB

product code MDB

Death: 6
Malfunction: 5,490
Total: 5,496

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.