Dannoritzer Medizintechnik GmbH & Co. KG
FDA Regulatory Profile
Dannoritzer Medizintechnik GmbH & Co. KG appears in FDA public data with 1 recall, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0062-2019, Class III) was initiated on August 6, 2018. Its most recent 510(k) clearance was granted on June 14, 2006.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-0062-2019 | Class III | Laparoscopy Instruments Instructions For Use (IFU) for the following: 1)Monopolar electrode, 2) Inse | August 6, 2018 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K052759 | DAN MONOPOLAR LAP ACCESSORIES | June 14, 2006 |