Last synced on 30 May 2025 at 11:05 pm

PENTAX Medical EPK-i7010 and PENTAX EPK-i5010 Video Processors with GI Family

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191282
510(k) Type
Traditional
Applicant
PENTAX of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2019
Days to Decision
179 days
Submission Type
Summary

PENTAX Medical EPK-i7010 and PENTAX EPK-i5010 Video Processors with GI Family

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191282
510(k) Type
Traditional
Applicant
PENTAX of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/2019
Days to Decision
179 days
Submission Type
Summary