Bladeless Trocar – Artemis Lap Cannula
K-Number: K230058 · 2023-04-28
Device Summary
Frequently Asked Questions
What is the Bladeless Trocar – Artemis Lap Cannula?
Bladeless Trocar – Artemis Lap Cannula is a medical device that received FDA 510(k) clearance on 2023-04-28. The listed applicant is T.A.G. Medical Products Corporation, Ltd.. The 510(k) number is K230058.
When did Bladeless Trocar – Artemis Lap Cannula receive FDA 510(k) clearance?
Bladeless Trocar – Artemis Lap Cannula received FDA 510(k) clearance on 2023-04-28, under 510(k) number K230058.
Who is the listed applicant for Bladeless Trocar – Artemis Lap Cannula?
The FDA 510(k) record lists T.A.G. Medical Products Corporation, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bladeless Trocar – Artemis Lap Cannula?
The FDA product code for Bladeless Trocar – Artemis Lap Cannula is GCJ.
Other records listing T.A.G. Medical Products Corporation, Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GCJ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.