510(k) K800025
K800025 is an FDA 510(k) premarket notification submitted by Applied Medical Research for the device "DINAMAP RESEARCH MONITOR 1245". The FDA issued a decision of Substantially Equivalent on February 1, 1980. The device falls under product code DXN (System, Measurement, Blood-Pressure, Non-Invasive), a Class II device regulated under 21 CFR 870.1130. Applied Medical Research has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 1, 1980
- Date Received
- January 7, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Measurement, Blood-Pressure, Non-Invasive
- Device Class
- Class II
- Regulation Number
- 870.1130
- Review Panel
- CV
- Submission Type