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Urethrotech UCD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190060
510(k) Type
Traditional
Applicant
Urethrotech
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/4/2019
Days to Decision
266 days
Submission Type
Summary

Urethrotech UCD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190060
510(k) Type
Traditional
Applicant
Urethrotech
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/4/2019
Days to Decision
266 days
Submission Type
Summary