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BOEHRINGER GASTRIC SIZING TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130483
510(k) Type
Traditional
Applicant
BOEHRINGER LABORATORIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2013
Days to Decision
31 days
Submission Type
Summary

BOEHRINGER GASTRIC SIZING TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130483
510(k) Type
Traditional
Applicant
BOEHRINGER LABORATORIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2013
Days to Decision
31 days
Submission Type
Summary