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NON-BALLOON REPLACEMENT GASTROSTOMY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915837
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
3/23/1993
Days to Decision
455 days
Submission Type
Summary

NON-BALLOON REPLACEMENT GASTROSTOMY SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915837
510(k) Type
Traditional
Applicant
C.R. BARD, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
3/23/1993
Days to Decision
455 days
Submission Type
Summary