Last synced on 9 May 2025 at 11:05 pm

Guidewire Locking Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220247
510(k) Type
Traditional
Applicant
Micro-Tech (Nanjing) Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/29/2022
Days to Decision
60 days
Submission Type
Summary

Guidewire Locking Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220247
510(k) Type
Traditional
Applicant
Micro-Tech (Nanjing) Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/29/2022
Days to Decision
60 days
Submission Type
Summary