Clearance Summary
HUNTLEIGH BETA II HM85 received FDA 510(k) clearance under submission number K870681, sponsored by Huntleigh Technology, Inc.. 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 1987-03-04.
- Submission: K870681
- Applicant / Sponsor: Huntleigh Technology, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5550
- Decision date: 1987-03-04
Classification & Regulation
This clearance is catalogued under FDA product code FNM and 21 CFR 880.5550, within the General Hospital review panel as a Class II device.