Last synced on 20 December 2024 at 11:05 pm

PENTAX Medical ED-3490TK Video Duodenoscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192280
510(k) Type
Traditional
Applicant
Pentax Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2019
Days to Decision
60 days
Submission Type
Summary

PENTAX Medical ED-3490TK Video Duodenoscope

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192280
510(k) Type
Traditional
Applicant
Pentax Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2019
Days to Decision
60 days
Submission Type
Summary