Clearance Summary
DIACROM *PLG received FDA 510(k) clearance under submission number K832591, sponsored by Wellcome Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1983-11-21.
- Submission: K832591
- Applicant / Sponsor: Wellcome Diagnostics
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class I
- Regulation citation: 21 CFR 866.5715
- Decision date: 1983-11-21
Classification & Regulation
This clearance is catalogued under FDA product code DDX and 21 CFR 866.5715, within the Immunology review panel as a Class I device.