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OMNIPORT HAND AND INSTRUMENT ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K011183
510(k) Type
Traditional
Applicant
Advanced Surgical Concepts (Asc)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2001
Days to Decision
58 days
Submission Type
Summary

OMNIPORT HAND AND INSTRUMENT ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K011183
510(k) Type
Traditional
Applicant
Advanced Surgical Concepts (Asc)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2001
Days to Decision
58 days
Submission Type
Summary