1
/
of
0
FDA 510(k), K150869, Checkme Pro Health Monitor
FDA 510(k), K150869, Checkme Pro Health Monitor
Regular price
$49.00 USD
Regular price
Sale price
$49.00 USD
Unit price
/
per
510(K) Number: K150869
Device Name: Checkme Pro Health Monitor
Manufacturer: Viatom Technology Co., Ltd.
Device Classification Name: monitor, physiological, patient (without arrhythmia detection or alarms)
Regulation Number: 870.2300
Classification Product Code: MWI
Date Received: 04/01/2015
Decision Date: 12/10/2015
Regulation Medical Specialty: Cardiovascular
Device Name: Checkme Pro Health Monitor
Manufacturer: Viatom Technology Co., Ltd.
Device Classification Name: monitor, physiological, patient (without arrhythmia detection or alarms)
Regulation Number: 870.2300
Classification Product Code: MWI
Date Received: 04/01/2015
Decision Date: 12/10/2015
Regulation Medical Specialty: Cardiovascular
Couldn't load pickup availability
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
View full details