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HUBER NEEDLE INFUSION SET MODEL #20G01 & Y-SITE MODEL #20G01Y

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981683
510(k) Type
Traditional
Applicant
Venusa , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1998
Days to Decision
76 days
Submission Type
Summary

HUBER NEEDLE INFUSION SET MODEL #20G01 & Y-SITE MODEL #20G01Y

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981683
510(k) Type
Traditional
Applicant
Venusa , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1998
Days to Decision
76 days
Submission Type
Summary