510(k) K113105
K113105 is an FDA 510(k) premarket notification submitted by Remote Diagnostic Technologies , Ltd. for the device "TEMPUSIC PATIENT MONITOR". The FDA issued a decision of Substantially Equivalent on December 15, 2011. 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. Remote Diagnostic Technologies , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 15, 2011
- Date Received
- October 20, 2011
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- Yes
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