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Eclipse DermaFlex Cannula

Page Type
Cleared 510(K)
510(k) Number
K200017
510(k) Type
Traditional
Applicant
Eclipse MedCorp, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2020
Days to Decision
307 days
Submission Type
Summary

Eclipse DermaFlex Cannula

Page Type
Cleared 510(K)
510(k) Number
K200017
510(k) Type
Traditional
Applicant
Eclipse MedCorp, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2020
Days to Decision
307 days
Submission Type
Summary