Clearance Summary
ELISA PLUS SYSTEM received FDA 510(k) clearance under submission number K830212, sponsored by William-Palmer Industries, 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 1983-04-05.
- Submission: K830212
- Applicant / Sponsor: William-Palmer Industries, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2160
- Decision date: 1983-04-05
Classification & Regulation
This clearance is catalogued under FDA product code JJE and 21 CFR 862.2160, within the Clinical Chemistry review panel as a Class I device.