Clearance Summary
GEMENI URIC ACID U.V. received FDA 510(k) clearance under submission number K873358, sponsored by Electro-Nucleonics Laboratories, 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 1987-09-11.
- Submission: K873358
- Applicant / Sponsor: Electro-Nucleonics Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1775
- Decision date: 1987-09-11
Classification & Regulation
This clearance is catalogued under FDA product code CDO and 21 CFR 862.1775, within the Clinical Chemistry review panel as a Class I device.