Clearance Summary
THE EXPANDACELL EAR PACK received FDA 510(k) clearance under submission number K940133, sponsored by Denver Splint Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1994-05-23.
- Submission: K940133
- Applicant / Sponsor: Denver Splint Co.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.5220
- Decision date: 1994-05-23
Classification & Regulation
This clearance is catalogued under FDA product code LRD and 21 CFR 874.5220, within the Ear, Nose, Throat review panel as a Class I device.