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CORTEK MINI LAPAROSCOPE

Page Type
Cleared 510(K)
510(k) Number
K000199
510(k) Type
Traditional
Applicant
CORTEK ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2000
Days to Decision
83 days
Submission Type
Statement

CORTEK MINI LAPAROSCOPE

Page Type
Cleared 510(K)
510(k) Number
K000199
510(k) Type
Traditional
Applicant
CORTEK ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2000
Days to Decision
83 days
Submission Type
Statement