Last synced on 25 January 2026 at 3:41 am

NovaCore Semi-Automatic Biopsy Instrument

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213232
510(k) Type
Traditional
Applicant
Argon Medical Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2022
Days to Decision
274 days
Submission Type
Summary

NovaCore Semi-Automatic Biopsy Instrument

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213232
510(k) Type
Traditional
Applicant
Argon Medical Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2022
Days to Decision
274 days
Submission Type
Summary