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ULTRASKIN HYDROPHILIC GUIDE WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141707
510(k) Type
Traditional
Applicant
LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2015
Days to Decision
211 days
Submission Type
Summary

ULTRASKIN HYDROPHILIC GUIDE WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141707
510(k) Type
Traditional
Applicant
LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/2015
Days to Decision
211 days
Submission Type
Summary