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PENTAX Medical Video Esophagoscope EE17-J10

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223072
510(k) Type
Traditional
Applicant
Pentax of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2022
Days to Decision
63 days
Submission Type
Summary

PENTAX Medical Video Esophagoscope EE17-J10

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223072
510(k) Type
Traditional
Applicant
Pentax of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2022
Days to Decision
63 days
Submission Type
Summary