Clearance Summary
ORLOCATE SYSTEM MODEL ORL 100 received FDA 510(k) clearance under submission number K100551, sponsored by Haldor Advanced Technologies, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2010-08-12.
- Submission: K100551
- Applicant / Sponsor: Haldor Advanced Technologies, Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.2740
- Decision date: 2010-08-12
Classification & Regulation
This clearance is catalogued under FDA product code LWH and 21 CFR 880.2740, within the General Hospital review panel as a Class I device.