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U-Blade Veress Needle

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162648
510(k) Type
Traditional
Applicant
Tianjin Uwell Medical Device Manufacturing Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/12/2016
Days to Decision
81 days
Submission Type
Summary

U-Blade Veress Needle

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162648
510(k) Type
Traditional
Applicant
Tianjin Uwell Medical Device Manufacturing Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/12/2016
Days to Decision
81 days
Submission Type
Summary