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SKYLARK URO PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053007
510(k) Type
Traditional
Applicant
SKYLARK DEVICE & SYSTEMS CO., LTD
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
12/5/2005
Days to Decision
40 days
Submission Type
Summary

SKYLARK URO PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053007
510(k) Type
Traditional
Applicant
SKYLARK DEVICE & SYSTEMS CO., LTD
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
12/5/2005
Days to Decision
40 days
Submission Type
Summary