510(k) K904220
K904220 is an FDA 510(k) premarket notification submitted by Beckman for the device "SYNCHRON CX4-CE". The FDA issued a decision of Substantially Equivalent on October 15, 1990. The device falls under product code JJE (Analyzer, Chemistry (Photometric, Discrete), For Clinical Use), a Class I device regulated under 21 CFR 862.2160. Beckman has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 15, 1990
- Date Received
- September 12, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Analyzer, Chemistry (Photometric, Discrete), For Clinical Use
- Device Class
- Class I
- Regulation Number
- 862.2160
- Review Panel
- CH
- Submission Type