510(k) K172510
K172510 is an FDA 510(k) premarket notification submitted by Zoll Manufacturing Corporation for the device "µCor Heart Failure and Arrhythmia Management System". The FDA issued a decision of Substantially Equivalent on May 11, 2018. The device falls under product code MHX (Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)), a Class II device regulated under 21 CFR 870.1025. Zoll Manufacturing Corporation has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 11, 2018
- Date Received
- Aug 21, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
- Device Class
- Class II
- Regulation Number
- 870.1025
- Review Panel
- CV
- Submission Type
- 510(k)