Clearance Summary
TRANSPHOR TM LD LACTATE DEHYDROGENASE received FDA 510(k) clearance under submission number K800568, sponsored by Corning Medical & Scientific. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1980-04-04.
- Submission: K800568
- Applicant / Sponsor: Corning Medical & Scientific
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1445
- Decision date: 1980-04-04
Classification & Regulation
This clearance is catalogued under FDA product code CFE and 21 CFR 862.1445, within the Clinical Chemistry review panel as a Class II device.