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CORTEK MINI LAPAROSCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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