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TriMed Ripcord Device

Page Type
Cleared 510(K)
510(k) Number
K220650
510(k) Type
Traditional
Applicant
TriMed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2022
Days to Decision
86 days
Submission Type
Summary

TriMed Ripcord Device

Page Type
Cleared 510(K)
510(k) Number
K220650
510(k) Type
Traditional
Applicant
TriMed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2022
Days to Decision
86 days
Submission Type
Summary