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VIVUS 50 AND VIVUS 100 PERSONAL INFUSER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915646
510(k) Type
Traditional
Applicant
I-FLOW CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1992
Days to Decision
180 days
Submission Type
Statement

VIVUS 50 AND VIVUS 100 PERSONAL INFUSER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915646
510(k) Type
Traditional
Applicant
I-FLOW CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/1992
Days to Decision
180 days
Submission Type
Statement