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LaparoLight Veress Needle

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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