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CORTEK LAPAROSCOPES

Page Type
Cleared 510(K)
510(k) Number
K000202
510(k) Type
Traditional
Applicant
CORTEK ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2000
Days to Decision
70 days
Submission Type
Statement

CORTEK LAPAROSCOPES

Page Type
Cleared 510(K)
510(k) Number
K000202
510(k) Type
Traditional
Applicant
CORTEK ENDOSCOPY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2000
Days to Decision
70 days
Submission Type
Statement