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DiscCath Needle Set

Page Type
Cleared 510(K)
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)
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