Clearance Summary
SARTOPHOR SYSTEM FOR ELECTROPHORESIS received FDA 510(k) clearance under submission number K823132, sponsored by Sartorius Filters, 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 1982-11-27.
- Submission: K823132
- Applicant / Sponsor: Sartorius Filters, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2485
- Decision date: 1982-11-27
Classification & Regulation
This clearance is catalogued under FDA product code JJN and 21 CFR 862.2485, within the Clinical Chemistry review panel as a Class I device.