Clearance Summary
LECTRO-LARYNX received FDA 510(k) clearance under submission number K923648, sponsored by Bruce Medical Supply. 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 1993-04-07.
- Submission: K923648
- Applicant / Sponsor: Bruce Medical Supply
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.3375
- Decision date: 1993-04-07
Classification & Regulation
This clearance is catalogued under FDA product code ESE and 21 CFR 874.3375, within the Ear, Nose, Throat review panel as a Class I device.