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FDA 510(k), K970456, HEWLETT APCKARD SERIES 50 OB TRACEVUE OBSTETRICAL SURVEILLANCE AND ARCHIVING SYSTEM
FDA 510(k), K970456, HEWLETT APCKARD SERIES 50 OB TRACEVUE OBSTETRICAL SURVEILLANCE AND ARCHIVING SYSTEM
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510(K) Number: K970456
Device Name: HEWLETT APCKARD SERIES 50 OB TRACEVUE OBSTETRICAL SURVEILLANCE AND ARCHIVING SYSTEM
Manufacturer: HEWLETT-PACKARD GMBH
Device Classification Name: System, Monitoring, Perinatal
Regulation Number: 884.2740
Classification Product Code: HGM
Date Received: 02/06/1997
Decision Date: 10/03/1997
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: HEWLETT APCKARD SERIES 50 OB TRACEVUE OBSTETRICAL SURVEILLANCE AND ARCHIVING SYSTEM
Manufacturer: HEWLETT-PACKARD GMBH
Device Classification Name: System, Monitoring, Perinatal
Regulation Number: 884.2740
Classification Product Code: HGM
Date Received: 02/06/1997
Decision Date: 10/03/1997
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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