Clearance Summary
DIA STRIPS SYSTEM received FDA 510(k) clearance under submission number K831623, sponsored by California Immuno Diagnostic, 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 1983-07-28.
- Submission: K831623
- Applicant / Sponsor: California Immuno Diagnostic, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.1785
- Decision date: 1983-07-28
Classification & Regulation
This clearance is catalogued under FDA product code CDM and 21 CFR 862.1785, within the Clinical Chemistry review panel as a Class I device.