510(k) K915200
K915200 is an FDA 510(k) premarket notification submitted by Becton Dickinson Advanced Diagnostics for the device "PRECISE TM HCG FOR USE IN THE PHYSICIANS OFFICE LA". The FDA issued a decision of Substantially Equivalent on December 16, 1991. The device falls under product code JHI (Visual, Pregnancy Hcg, Prescription Use), a Class II device regulated under 21 CFR 862.1155. Becton Dickinson Advanced Diagnostics has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 16, 1991
- Date Received
- November 19, 1991
- 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