FDA device listing
1088 1288 1488,1588 AIM Camera Extension Cable, 20ft,1588 AIM CAMERA HEAD, C-MOUNT,1588 AIM CAMERA HEAD WITH INTEGRATED…
FDA device listing 1539338653 · STRYKER CORP.
Key facts
| Proprietary names | 1088 1288 1488,1588 AIM Camera Extension Cable, 20ft,1588 AIM CAMERA HEAD, C-MOUNT,1588 AIM CAMERA HEAD WITH INTEGRATED COUPLER,1588 AIM INLINE CAMERA HEAD, C-MOUNT,1588 PENDULUM CAMERA HEAD WITH INTEGRATED COUPLER |
|---|---|
| Owner/operator | STRYKER CORP. |
| Owner/operator number | 1811755 |
| Premarket submissions | K132785 |
| Product codes | GCJ |
| Device names | GCJ - Laparoscope, General & Plastic Surgery |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.1500 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | STRYKER ENDOSCOPY |
| Establishment registrations | 2936485 |
| FEI numbers | 2936485 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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