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ENDO VIVE STANDARD REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083684
510(k) Type
Traditional
Applicant
MANUFACTURING & RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2009
Days to Decision
55 days
Submission Type
Summary

ENDO VIVE STANDARD REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K083684
510(k) Type
Traditional
Applicant
MANUFACTURING & RESEARCH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2009
Days to Decision
55 days
Submission Type
Summary