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KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA

Page Type
Cleared 510(K)
510(k) Number
K950282
510(k) Type
Traditional
Applicant
KARL STORZ ENDOSCOPY-AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1995
Days to Decision
71 days
Submission Type
Summary

KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA

Page Type
Cleared 510(K)
510(k) Number
K950282
510(k) Type
Traditional
Applicant
KARL STORZ ENDOSCOPY-AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/1995
Days to Decision
71 days
Submission Type
Summary