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Triopsy Actuator (TMSDGB); Triopsy Biopsy Needle (BN-1825-36-01); Triopsy Biopsy Needle (BN-1825-55-01)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242228
510(k) Type
Traditional
Applicant
Triopsy Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2025
Days to Decision
164 days
Submission Type
Summary

Triopsy Actuator (TMSDGB); Triopsy Biopsy Needle (BN-1825-36-01); Triopsy Biopsy Needle (BN-1825-55-01)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242228
510(k) Type
Traditional
Applicant
Triopsy Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2025
Days to Decision
164 days
Submission Type
Summary