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Pentax Medical Video Duodenoscope ED34-i10T2

Page Type
Cleared 510(K)
510(k) Number
K192245
510(k) Type
Traditional
Applicant
PENTAX of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2019
Days to Decision
88 days
Submission Type
Summary

Pentax Medical Video Duodenoscope ED34-i10T2

Page Type
Cleared 510(K)
510(k) Number
K192245
510(k) Type
Traditional
Applicant
PENTAX of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2019
Days to Decision
88 days
Submission Type
Summary