Clearance Summary
NASOGRASTRIC TUBBE HOLDER received FDA 510(k) clearance under submission number K922209, sponsored by Innovative Medical Design Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1992-10-30.
- Submission: K922209
- Applicant / Sponsor: Innovative Medical Design Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5980
- Decision date: 1992-10-30
Classification & Regulation
This clearance is catalogued under FDA product code KNT and 21 CFR 876.5980, within the Gastroenterology, Urology review panel as a Class II device.