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B. Braun/Mcgaw
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K994111
CELSITE, MODELS ST401L, ST405L
January 3, 2000
K983373
IMPACT BALLOON DILATION CATHETER
June 22, 1999