Last synced on 25 November 2022 at 11:04 pm

Diathermic Slitter (FlushKnife) DK2620JI and DK2623JI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220053
510(k) Type
Special
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
2/4/2022
Days to Decision
29 days
Submission Type
Summary

Diathermic Slitter (FlushKnife) DK2620JI and DK2623JI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220053
510(k) Type
Special
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
2/4/2022
Days to Decision
29 days
Submission Type
Summary