BD Phoenix Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL)
K-Number: K250447 · 2025-05-19
Device Summary
Frequently Asked Questions
What is the BD Phoenix Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL)?
BD Phoenix Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL) is a medical device that received FDA 510(k) clearance on 2025-05-19. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K250447.
When was BD Phoenix Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL) approved by the FDA?
BD Phoenix Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL) received FDA 510(k) clearance on 2025-05-19, under approval number K250447.
What company makes BD Phoenix Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL)?
BD Phoenix Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL) is manufactured by Becton, Dickinson and Company.
What is the FDA product code for BD Phoenix Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL)?
The FDA product code for BD Phoenix Automated Microbiology System - GN Imipenem-relebactam (0.0625/4 - 16/4 µg/mL) is LON.
Related Clinical Trials
Related PubMed Literature
Other Devices by Becton, Dickinson and Company
Related Devices (Code: LON)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.