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Uramix CuraWay Biopsy Needle

Page Type
Cleared 510(K)
510(k) Number
K203141
510(k) Type
Traditional
Applicant
Uramix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2021
Days to Decision
332 days
Submission Type
Summary

Uramix CuraWay Biopsy Needle

Page Type
Cleared 510(K)
510(k) Number
K203141
510(k) Type
Traditional
Applicant
Uramix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2021
Days to Decision
332 days
Submission Type
Summary