510(k) K112921
K112921 is an FDA 510(k) premarket notification submitted by Medicalgorithmics S.A. for the device "MEDICALGORITHMICS UNIFIED ARRHYTHMIA DIAGNOSTIC SYSTEM". The FDA issued a decision of Substantially Equivalent on May 16, 2012. The device falls under product code DSI (Detector And Alarm, Arrhythmia), a Class II device regulated under 21 CFR 870.1025. Medicalgorithmics S.A. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 16, 2012
- Date Received
- October 3, 2011
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Detector And Alarm, Arrhythmia
- Device Class
- Class II
- Regulation Number
- 870.1025
- Review Panel
- CV
- Submission Type