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COMBIPROT EMERGENCY ENFUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K970359
510(k) Type
Traditional
Applicant
B. BRAUN MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1997
Days to Decision
46 days
Submission Type
Summary

COMBIPROT EMERGENCY ENFUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K970359
510(k) Type
Traditional
Applicant
B. BRAUN MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1997
Days to Decision
46 days
Submission Type
Summary