510(k) K924259
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 25, 1992
- Date Received
- August 24, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Visual, Pregnancy Hcg, Prescription Use
- Device Class
- Class II
- Regulation Number
- 862.1155
- Review Panel
- CH
- Submission Type