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PENTAX Medical Video Colonoscope (EC38-i20cWL)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242110
510(k) Type
Traditional
Applicant
Pentax of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2025
Days to Decision
168 days
Submission Type
Summary

PENTAX Medical Video Colonoscope (EC38-i20cWL)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242110
510(k) Type
Traditional
Applicant
Pentax of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/3/2025
Days to Decision
168 days
Submission Type
Summary