510(k) K031886
K031886 is an FDA 510(k) premarket notification submitted by Medison Co., Ltd. for the device "SONOVIEW PRO BY MEDISON CO., LTD.". The FDA issued a decision of Substantially Equivalent on June 30, 2003. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Medison Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 30, 2003
- Date Received
- June 18, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, Image Processing, Radiological
- Device Class
- Class II
- Regulation Number
- 892.2050
- Review Panel
- RA
- Submission Type