510(k) K870233
K870233 is an FDA 510(k) premarket notification submitted by Abbott Diagnostics for the device "CELL-DYN 1600 MULTIPARAMETER AUTO. HEMA. ANALYZER". The FDA issued a decision of Substantially Equivalent on March 17, 1987. The device falls under product code GKZ (Counter, Differential Cell), a Class II device regulated under 21 CFR 864.5220. Abbott Diagnostics has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 17, 1987
- Date Received
- January 21, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Counter, Differential Cell
- Device Class
- Class II
- Regulation Number
- 864.5220
- Review Panel
- HE
- Submission Type