Last synced on 21 June 2024 at 11:04 pm

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
K231400
510(k) Type
Special
Applicant
T.A.G. Medical Products Corporation, Ltd
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/4/2023
Days to Decision
81 days
Submission Type
Summary