FFZ
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Cord, Electric, For Endoscope
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1500
- Medical specialty
- Gastroenterology, Urology
- Adverse events (MAUDE)
- 2001: 5 · 2002: 2 · 2003: 6 · 2004: 3 · 2005: 10 · 2007: 7
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ACEM (K111013) | Sandhill Scientific, Inc. | 2011-12-19 |
| ELECTRIC CORD FOR ENDOSCOPE (K822254) | Kelleher Corp. | 1982-08-20 |
| C-CORD (K782046) | Concept, Inc. | 1979-01-10 |
Track FFZ automatically
Every clearance here is in the API, with alerts when new ones post.