Clearance Summary
APEX LOCATOR BINGO-1020 received FDA 510(k) clearance under submission number K992233, sponsored by Dent Corp. Research & Development. The device was reviewed via the Traditional premarket notification pathway and assigned to the Unknown review panel. The statutory decision date of record is 1999-11-30.
- Submission: K992233
- Applicant / Sponsor: Dent Corp. Research & Development
- Clearance pathway: Traditional
- Review panel: Unknown
- Device class:
- Decision date: 1999-11-30
Classification & Regulation
This clearance is catalogued under FDA product code LQY , within the Unknown review panel as a device.