Fehling Instruments GmbH & Co. KG
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K170726 | Biopsy Forceps | June 2, 2017 |
| K153243 | Fehling-Punches | August 4, 2016 |