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Needle Stimulator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202861
510(k) Type
Traditional
Applicant
Wuxi Jiajian Medical Instrument Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
8/27/2021
Days to Decision
333 days
Submission Type
Summary

Needle Stimulator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202861
510(k) Type
Traditional
Applicant
Wuxi Jiajian Medical Instrument Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
8/27/2021
Days to Decision
333 days
Submission Type
Summary