510(k) K112755
K112755 is an FDA 510(k) premarket notification submitted by Diatron U.S., Inc. for the device "ABACUS 5". The FDA issued a decision of Substantially Equivalent on March 27, 2012. The device falls under product code GKZ (Counter, Differential Cell), a Class II device regulated under 21 CFR 864.5220. Diatron U.S., Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 27, 2012
- Date Received
- September 21, 2011
- 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