Clearance Summary
VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM received FDA 510(k) clearance under submission number K851945, sponsored by Varian Assoc., 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 1985-05-24.
- Submission: K851945
- Applicant / Sponsor: Varian Assoc., Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2260
- Decision date: 1985-05-24
Classification & Regulation
This clearance is catalogued under FDA product code KZR and 21 CFR 862.2260, within the Clinical Chemistry review panel as a Class I device.