Last synced on 13 May 2022 at 11:05 pm

DiscCath Needle Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212328
510(k) Type
Traditional
Applicant
DiscCath LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2021
Days to Decision
61 days
Submission Type
Summary

DiscCath Needle Set

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212328
510(k) Type
Traditional
Applicant
DiscCath LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2021
Days to Decision
61 days
Submission Type
Summary