510(k) K002067
K002067 is an FDA 510(k) premarket notification submitted by Radi Medical Systems AB for the device "RADIANALYZER, MODEL 12710". The FDA issued a decision of Substantially Equivalent on January 11, 2001. The device falls under product code DSK (Computer, Blood-Pressure), a Class II device regulated under 21 CFR 870.1110. Radi Medical Systems AB has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 11, 2001
- Date Received
- July 7, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Computer, Blood-Pressure
- Device Class
- Class II
- Regulation Number
- 870.1110
- Review Panel
- CV
- Submission Type