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F. Walter Hanel GmbH
FDA Regulatory Profile
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