Cook Endoscopy
FDA Regulatory Profile
Cook Endoscopy appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 5, 2020.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K192697 | Instinct Plus Endoscopic Clipping Device | March 5, 2020 |
| K090183 | HERCULES 3 STAGE WIRE GUIDED DILATION BALLOON | September 25, 2009 |
| K083330 | ECHOTIP ULTRA ULTRASOUND NEEDLE | February 6, 2009 |
| K061937 | COOK ENDOSCOPY ESOPHAGEAL DILATION BALLOON | December 1, 2006 |