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FDA 510(k), K112911, FETAL DOPPLER
FDA 510(k), K112911, FETAL DOPPLER
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510(K) Number: K112911
Device Name: FETAL DOPPLER
Manufacturer: BEIJING CHOICE ELECTRONIC TECHNOLOLGY CO., LTD.
Device Classification Name: monitor, ultrasonic, fetal
Regulation Number: 884.2660
Classification Product Code: KNG
Date Received: 10/03/2011
Decision Date: 10/27/2011
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: FETAL DOPPLER
Manufacturer: BEIJING CHOICE ELECTRONIC TECHNOLOLGY CO., LTD.
Device Classification Name: monitor, ultrasonic, fetal
Regulation Number: 884.2660
Classification Product Code: KNG
Date Received: 10/03/2011
Decision Date: 10/27/2011
Regulation Medical Specialty: Obstetrics/Gynecology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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.
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