FJQ
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Connector, Shunt
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 876.5540
- Medical specialty
- Gastroenterology, Urology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SHUNT CONNECTORS (K893679) | Akcess Medical Products, Inc. | 1989-07-24 |
| PATIENT BY-PASS (K771422) | Quinton, Inc. | 1978-01-03 |
| DISP. TEFLON CONNHCTOR (K771429) | Quinton, Inc. | 1977-12-22 |
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Every clearance here is in the API, with alerts when new ones post.