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FDA 510(k), K142583, LaborView LV1000
FDA 510(k), K142583, LaborView LV1000
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510(K) Number: K142583
Device Name: LaborView LV1000
Manufacturer: OBMedical Company
Device Classification Name: uterine electromyographic monitor
Regulation Number: 884.2720
Classification Product Code: OSP
Date Received: 09/15/2014
Decision Date: 01/16/2015
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: LaborView LV1000
Manufacturer: OBMedical Company
Device Classification Name: uterine electromyographic monitor
Regulation Number: 884.2720
Classification Product Code: OSP
Date Received: 09/15/2014
Decision Date: 01/16/2015
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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