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FDA 510(k), K131457, FETAL ULTRASONIC MONITOR AND ACCESSORIES
FDA 510(k), K131457, FETAL ULTRASONIC MONITOR AND ACCESSORIES
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510(K) Number: K131457
Device Name: FETAL ULTRASONIC MONITOR AND ACCESSORIES
Manufacturer: SHENZHEN JUMPER MEDICAL EQUIPMENT CO., LTD
Device Classification Name: monitor, ultrasonic, fetal
Regulation Number: 884.2660
Classification Product Code: KNG
Date Received: 05/20/2013
Decision Date: 01/24/2014
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: FETAL ULTRASONIC MONITOR AND ACCESSORIES
Manufacturer: SHENZHEN JUMPER MEDICAL EQUIPMENT CO., LTD
Device Classification Name: monitor, ultrasonic, fetal
Regulation Number: 884.2660
Classification Product Code: KNG
Date Received: 05/20/2013
Decision Date: 01/24/2014
Regulation Medical Specialty: Obstetrics/Gynecology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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