Clearance Summary
LITH A TEST TM received FDA 510(k) clearance under submission number K830091, sponsored by Lenal Creative Approaches, Inc.. 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 1983-02-15.
- Submission: K830091
- Applicant / Sponsor: Lenal Creative Approaches, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1550
- Decision date: 1983-02-15
Classification & Regulation
This clearance is catalogued under FDA product code CEN and 21 CFR 862.1550, within the Clinical Chemistry review panel as a Class I device.