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LaparoLight Veress Needle

Page Type
Cleared 510(K)
510(k) Number
K171139
510(k) Type
Traditional
Applicant
Buffalo Filter, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2017
Days to Decision
30 days
Submission Type
Summary

LaparoLight Veress Needle

Page Type
Cleared 510(K)
510(k) Number
K171139
510(k) Type
Traditional
Applicant
Buffalo Filter, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2017
Days to Decision
30 days
Submission Type
Summary