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ENTUIT THRIVE BALLOON RETENTION GASTROSTOMY FEEDING TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130611
510(k) Type
Traditional
Applicant
XERIDIEM MEDICAL DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2013
Days to Decision
287 days
Submission Type
Summary