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CORTEK URETHEROSCOPE

Page Type
Cleared 510(K)
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)
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