510(k) K960827
K960827 is an FDA 510(k) premarket notification submitted by Becton Dickinson Diagnostic Instrument Systems for the device "QBC ACCUTUBE(423406)/QBC AUTOREAD(424571)". The FDA issued a decision of Substantially Equivalent on May 17, 1996. The device falls under product code GKZ (Counter, Differential Cell), a Class II device regulated under 21 CFR 864.5220. Becton Dickinson Diagnostic Instrument Systems has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 17, 1996
- Date Received
- February 29, 1996
- 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