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ENDOPATH ULTRA-RETRACTOR/ ENDOPATH VESSEL DISSECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K973139
510(k) Type
Traditional
Applicant
ETHICON ENDO-SURGERY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1997
Days to Decision
84 days
Submission Type
Summary