510(k) K983071
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 4, 1999
- Date Received
- September 2, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bilirubin (Total And Unbound) In The Neonate Test System
- Device Class
- Class I
- Regulation Number
- 862.1113
- Review Panel
- CH
- Submission Type