FDA device listing
BD Kiestra™ ID AST Calibrator Kit,BD Phoenix™ AP,BD PhoenixSpec™ AP Calibrator Kit,BD PhoenixSpec™ Calibrator 0.25…
FDA device listing 1438994390 · Becton Dickinson and Company
Key facts
| Proprietary names | BD Kiestra™ ID AST Calibrator Kit,BD Phoenix™ AP,BD PhoenixSpec™ AP Calibrator Kit,BD PhoenixSpec™ Calibrator 0.25 McFarland,BD PhoenixSpec™ Calibrator 0.50 McFarland,BD PhoenixSpec™ Calibrator 2.0 McFarland,BD PhoenixSpec™ Calibrator Kit,BD PhoenixSpec™ Nephelometer |
|---|---|
| Owner/operator | Becton Dickinson and Company |
| Owner/operator number | 9922032 |
| Product codes | JQX |
| Device names | JQX - Nephelometer, For Clinical Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2700 |
| Review panels | Clinical Chemistry |
| Registered establishments | BECTON, DICKINSON & CO. |
| Establishment registrations | 1111096, 1119779 |
| FEI numbers | 1111096, 1119779 |
| Establishment operations | Complaint File Establishment, Manufacturer, Repackager/Relabeler, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database