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FDA 510(k)

BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL)

K-Number: K233986 · 2024-03-15

Decision Date2024-03-15
Product CodeLON
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL) is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2024-03-15 under approval number K233986. The device is classified under product code LON. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL)?

BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL) is a medical device that received FDA 510(k) clearance on 2024-03-15. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K233986.

When was BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL) approved by the FDA?

BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL) received FDA 510(k) clearance on 2024-03-15, under approval number K233986.

What company makes BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL)?

BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL) is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL)?

The FDA product code for BD Phoenix™ Automated Microbiology System - GN Ciprofloxacin (0.0156–4 µg/mL) is LON.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.