Clearance Summary
DI CUSTOM IN THE EAR AND IN THE CANAL received FDA 510(k) clearance under submission number K920657, sponsored by Dakota Laboratories, Inc.. 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 1992-03-31.
- Submission: K920657
- Applicant / Sponsor: Dakota Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.3300
- Decision date: 1992-03-31
Classification & Regulation
This clearance is catalogued under FDA product code ESD and 21 CFR 874.3300, within the Ear, Nose, Throat review panel as a Class I device.