Last synced on 2 December 2022 at 11:04 pm

PENTEX EC-3890LI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093037
510(k) Type
Traditional
Applicant
PENTAX MEDICAL COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/2009
Days to Decision
90 days
Submission Type
Summary

PENTEX EC-3890LI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093037
510(k) Type
Traditional
Applicant
PENTAX MEDICAL COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/2009
Days to Decision
90 days
Submission Type
Summary