Clearance Summary
QUANTECH MYOGLOBIN ASSAY received FDA 510(k) clearance under submission number K981536, sponsored by Hellen Professional Services. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1998-06-29.
- Submission: K981536
- Applicant / Sponsor: Hellen Professional Services
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5680
- Decision date: 1998-06-29
Classification & Regulation
This clearance is catalogued under FDA product code MVE and 21 CFR 866.5680, within the Immunology review panel as a Class II device.