510(k) K810028
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 16, 1981
- Date Received
- January 6, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sampler, Blood, Fetal
- Device Class
- Class II
- Regulation Number
- 884.1560
- Review Panel
- OB
- Submission Type