Becton Dickinson
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K243062 | BD Intelliport System; BD Intelliport Reader (516230); BD Intelliport Sensor (516229); BD Intelliport Gateway (516232); BD Intelliport Mount (516233); BD Intelliport Charger (516231) | PHC | 2025-06-20 | View |
| 510(k) | K161810 | BD BACTEC Standard/10 Aerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial | MDB | 2017-02-09 | View |
| 510(k) | K161306 | BD BACTEC Standard Anaerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial | MDB | 2016-08-08 | View |
| 510(k) | K113241 | BD EMERALD SINGLE USE, HYPODERMIC SYRINGE | FMF | 2011-11-28 | View |
| 510(k) | K041478 | BD LOGIC BLOOD GLUCOSE MONITOR AND PARADIGM LINK BLOOD GLUCOSE MONITOR | CGA | 2004-10-28 | View |
| 510(k) | K042061 | 0.9% SODIUM CHLORIDE INJECTION, USP BD POSTFLUSH SF FLUSH SYRINGE | NGT | 2004-08-26 | View |
No matching devices.
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