510(k) K993333
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 16, 1999
- Date Received
- October 4, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Test, Pregnancy, Hcg, Over The Counter
- Device Class
- Class II
- Regulation Number
- 862.1155
- Review Panel
- CH
- Submission Type