CORGRIP* SR NG/NI Tube Retention System
K-Number: K241185 · 2024-10-25
Device Summary
Frequently Asked Questions
What is the CORGRIP* SR NG/NI Tube Retention System?
CORGRIP* SR NG/NI Tube Retention System is a medical device that received FDA 510(k) clearance on 2024-10-25. The listed applicant is Avanos Medical, Inc.. The 510(k) number is K241185.
When did CORGRIP* SR NG/NI Tube Retention System receive FDA 510(k) clearance?
CORGRIP* SR NG/NI Tube Retention System received FDA 510(k) clearance on 2024-10-25, under 510(k) number K241185.
Who is the listed applicant for CORGRIP* SR NG/NI Tube Retention System?
The FDA 510(k) record lists Avanos Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CORGRIP* SR NG/NI Tube Retention System?
The FDA product code for CORGRIP* SR NG/NI Tube Retention System is KNT.
Other records listing Avanos Medical, Inc. 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: KNT)
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.