Hans Pausch Rontgengeratebau Gmbh
Hans Pausch Rontgengeratebau Gmbh appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2152-2017, Class II) was initiated on March 14, 2017.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2152-2017 | Class II | Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040 Primarily for urological | March 14, 2017 |