Clearance Summary
LAS-R HUMAN PLASMINOGEN TEST received FDA 510(k) clearance under submission number K772085, sponsored by Hyland Therapeutic Div., Travenol Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1978-01-24.
- Submission: K772085
- Applicant / Sponsor: Hyland Therapeutic Div., Travenol Laboratories
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class I
- Regulation citation: 21 CFR 866.5715
- Decision date: 1978-01-24
Classification & Regulation
This clearance is catalogued under FDA product code DDX and 21 CFR 866.5715, within the Immunology review panel as a Class I device.