Clearance Summary
ORL-E-92 SURGICAL DRILL SYSTEM received FDA 510(k) clearance under submission number K984244, sponsored by Bien Air USA, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1999-02-23.
- Submission: K984244
- Applicant / Sponsor: Bien Air USA, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 1999-02-23
Classification & Regulation
This clearance is catalogued under FDA product code EFB and 21 CFR 872.4200, within the Dental review panel as a Class I device.