F. Walter Hanel GmbH
FDA Regulatory Profile
F. Walter Hanel GmbH appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 29, 1996.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K954945 | HANEL MAVIG MONITOR SUSPENSION SYSTEM | January 29, 1996 |
| K945238 | MAVIG LOWER BODY PROTECTION SYSTEMS, ASSEMBLY MODELS 6265, 6266, 6267, 6268, 6269/0, 629/1, AND 6269 | December 15, 1994 |
| K934206 | MAVIG ANGIO SHIELD MODELS 6290 & 6272 | October 7, 1993 |