510(k) K172965
K172965 is an FDA 510(k) premarket notification submitted by Visiomed Technology Co.,Ltd for the device "Handheld VitalSigns Monitoring System". The FDA issued a decision of Substantially Equivalent on Dec 17, 2018. The device falls under product code MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)), a Class II device regulated under 21 CFR 870.2300.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 17, 2018
- Date Received
- Sep 26, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
- Device Class
- Class II
- Regulation Number
- 870.2300
- Review Panel
- CV
- Submission Type
- 510(k)