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KSEA INSTRUMENT SET FOR SAPHENOUS VEIN HARVESTING

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973068
510(k) Type
Traditional
Applicant
KARL STORZ ENDOSKOP GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1997
Days to Decision
81 days
Submission Type
Summary