Last synced on 30 May 2025 at 11:05 pm

KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA

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