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CORTEK URETHEROSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000200
510(k) Type
Traditional
Applicant
CORTEK ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2000
Days to Decision
42 days
Submission Type
Summary

CORTEK URETHEROSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000200
510(k) Type
Traditional
Applicant
CORTEK ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/3/2000
Days to Decision
42 days
Submission Type
Summary