Last synced on 19 July 2024 at 11:05 pm

EG-3630UR, ULTRASUND VIDEO GASTROSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013640
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2002
Days to Decision
91 days
Submission Type
Summary

EG-3630UR, ULTRASUND VIDEO GASTROSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013640
510(k) Type
Traditional
Applicant
PENTAX PRECISION INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/2002
Days to Decision
91 days
Submission Type
Summary