Clearance Summary
DETECTOR, MODEL 79875A, VARIABLE received FDA 510(k) clearance under submission number K781771, sponsored by Hewlett-Packard Co.. 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 1978-12-20.
- Submission: K781771
- Applicant / Sponsor: Hewlett-Packard Co.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2260
- Decision date: 1978-12-20
Classification & Regulation
This clearance is catalogued under FDA product code KIE and 21 CFR 862.2260, within the Clinical Chemistry review panel as a Class I device.