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
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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