510(k) K951753
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 17, 1995
- Date Received
- April 17, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Station, Pipetting And Diluting, For Clinical Use
- Device Class
- Class I
- Regulation Number
- 862.2750
- Review Panel
- CH
- Submission Type