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PENTAX EG-3870UTK ULTRASOUND VIDEO GASTROSCOPE + HI VISION PREIRUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130247
510(k) Type
Special
Applicant
PENTAX OF AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2013
Days to Decision
47 days
Submission Type
Summary

PENTAX EG-3870UTK ULTRASOUND VIDEO GASTROSCOPE + HI VISION PREIRUS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130247
510(k) Type
Special
Applicant
PENTAX OF AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2013
Days to Decision
47 days
Submission Type
Summary