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Endo Vive 3S Low Profile Balloon Kit, Endo Vive 3S Bolus Extension Sets, Endo Vive 3S Continuous Extension Sets, Endo Vive 3S Medication Extension Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142297
510(k) Type
Traditional
Applicant
XERIDIEM (FORMERLY MRI)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2015
Days to Decision
143 days
Submission Type
Summary

Endo Vive 3S Low Profile Balloon Kit, Endo Vive 3S Bolus Extension Sets, Endo Vive 3S Continuous Extension Sets, Endo Vive 3S Medication Extension Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142297
510(k) Type
Traditional
Applicant
XERIDIEM (FORMERLY MRI)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2015
Days to Decision
143 days
Submission Type
Summary