510(k) K030799
K030799 is an FDA 510(k) premarket notification submitted by Abx Diagnostics for the device "MICROS 60". The FDA issued a decision of Substantially Equivalent on April 8, 2003. The device falls under product code GKZ (Counter, Differential Cell), a Class II device regulated under 21 CFR 864.5220. Abx Diagnostics has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 8, 2003
- Date Received
- March 13, 2003
- Clearance Type
- Special
- 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