Clearance Summary
SYNCHRON CX3 DELTA received FDA 510(k) clearance under submission number K942676, sponsored by Beckman-Diagnostic Systems Group. 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 1994-11-02.
- Submission: K942676
- Applicant / Sponsor: Beckman-Diagnostic Systems Group
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class I
- Regulation citation: 21 CFR 862.2170
- Decision date: 1994-11-02
Classification & Regulation
This clearance is catalogued under FDA product code JJF and 21 CFR 862.2170, within the Clinical Chemistry review panel as a Class I device.