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ENDOPATH ULTRA VERESS NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K983925
510(k) Type
Traditional
Applicant
ETHICON ENDO-SURGERY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1999
Days to Decision
90 days
Submission Type
Summary

ENDOPATH ULTRA VERESS NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K983925
510(k) Type
Traditional
Applicant
ETHICON ENDO-SURGERY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1999
Days to Decision
90 days
Submission Type
Summary