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ESOPHAGEAL OVERTUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890629
510(k) Type
Traditional
Applicant
GASTROTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1989
Days to Decision
110 days

ESOPHAGEAL OVERTUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K890629
510(k) Type
Traditional
Applicant
GASTROTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1989
Days to Decision
110 days