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Automatic Core Biopsy Instrument/ Semi-Automatic Core Biopsy Instrument/ Disposable Coaxial Biopsy Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241793
510(k) Type
Traditional
Applicant
Zhejiang CuraWay Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/24/2025
Days to Decision
217 days
Submission Type
Summary

Automatic Core Biopsy Instrument/ Semi-Automatic Core Biopsy Instrument/ Disposable Coaxial Biopsy Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241793
510(k) Type
Traditional
Applicant
Zhejiang CuraWay Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/24/2025
Days to Decision
217 days
Submission Type
Summary