FDA device listing
Chest Piece,Precordial Chest Piece,Precordial Stethoscope,Stethoscope
FDA device listing 1793067894 · Anesthesia Associates, Inc
Key facts
| Proprietary names | Chest Piece,Precordial Chest Piece,Precordial Stethoscope,Stethoscope |
|---|---|
| Owner/operator | Anesthesia Associates, Inc |
| Owner/operator number | 2022648 |
| Product codes | BZS |
| Device names | BZS - Stethoscope Head |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.1930 |
| Review panels | Anesthesiology |
| Registered establishments | Anesthesia Associates, Inc. |
| Establishment registrations | 2022648 |
| FEI numbers | 2022648 |
| Establishment operations | Contract Manufacturer, Manufacturer, Repackager/Relabeler |
| 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