Clearance Summary
TIBC PRETREATMENT KIT received FDA 510(k) clearance under submission number K842019, sponsored by E.I. Dupont DE Nemours & Co., 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 1984-06-22.
- Submission: K842019
- Applicant / Sponsor: E.I. Dupont DE Nemours & Co., Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1415
- Decision date: 1984-06-22
Classification & Regulation
This clearance is catalogued under FDA product code JQE and 21 CFR 862.1415, within the Clinical Chemistry review panel as a Class I device.