K241185
- 510(k) number
- K241185
- Device name
- CORGRIP* SR NG/NI Tube Retention System
- Applicant
- Avanos Medical, Inc. GA · US
- Product code
- KNT — Tubes, Gastrointestinal (And Accessories)
- Decision date
- 2024-10-25
- Date received
- 2024-04-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K241185
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.