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COMBIPROT EMERGENCY ENFUSION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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