Last synced on 14 November 2025 at 11:06 pm

SUREcore Plus Biopsy Instrument

Page Type
Cleared 510(K)
510(k) Number
K220611
510(k) Type
Traditional
Applicant
Uro-1, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2022
Days to Decision
274 days
Submission Type
Summary

SUREcore Plus Biopsy Instrument

Page Type
Cleared 510(K)
510(k) Number
K220611
510(k) Type
Traditional
Applicant
Uro-1, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2022
Days to Decision
274 days
Submission Type
Summary