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KDL Angiography Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201929
510(k) Type
Traditional
Applicant
Shanghai Kindly Medical Instruments Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/14/2021
Days to Decision
308 days
Submission Type
Summary

KDL Angiography Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201929
510(k) Type
Traditional
Applicant
Shanghai Kindly Medical Instruments Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/14/2021
Days to Decision
308 days
Submission Type
Summary