Clearance Summary
THROAT MOI-STIR received FDA 510(k) clearance under submission number K840807, sponsored by Kingswood Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Unknown review panel. The statutory decision date of record is 1984-05-25.
- Submission: K840807
- Applicant / Sponsor: Kingswood Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Unknown
- Device class:
- Decision date: 1984-05-25
Classification & Regulation
This clearance is catalogued under FDA product code LFD , within the Unknown review panel as a device.