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Bladeless Trocar – Artemis Lap Cannula

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230058
510(k) Type
Traditional
Applicant
T.A.G. Medical Products Corporation, Ltd
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
4/28/2023
Days to Decision
109 days
Submission Type
Summary