Niti-S Duodenal Stent; Niti-S Colonic Comfort Stent
K-Number: K223067 · 2023-06-14
Device Summary
Frequently Asked Questions
What is the Niti-S Duodenal Stent; Niti-S Colonic Comfort Stent?
Niti-S Duodenal Stent; Niti-S Colonic Comfort Stent is a medical device that received FDA 510(k) clearance on 2023-06-14. The listed applicant is Taewoong Medical Co., Ltd.. The 510(k) number is K223067.
When did Niti-S Duodenal Stent; Niti-S Colonic Comfort Stent receive FDA 510(k) clearance?
Niti-S Duodenal Stent; Niti-S Colonic Comfort Stent received FDA 510(k) clearance on 2023-06-14, under 510(k) number K223067.
Who is the listed applicant for Niti-S Duodenal Stent; Niti-S Colonic Comfort Stent?
The FDA 510(k) record lists Taewoong Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Niti-S Duodenal Stent; Niti-S Colonic Comfort Stent?
The FDA product code for Niti-S Duodenal Stent; Niti-S Colonic Comfort Stent is MUM.
Other records listing Taewoong Medical Co., 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: MUM)
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.