Clearance Summary
LDH REAGENT SET received FDA 510(k) clearance under submission number K812836, sponsored by Anco Medical Reagents & Assoc.. 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 1981-10-09.
- Submission: K812836
- Applicant / Sponsor: Anco Medical Reagents & Assoc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1440
- Decision date: 1981-10-09
Classification & Regulation
This clearance is catalogued under FDA product code CFH and 21 CFR 862.1440, within the Clinical Chemistry review panel as a Class II device.