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FDA 510(k), K090061, AIRSTRIP OB
FDA 510(k), K090061, AIRSTRIP OB
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510(K) Number: K090061
Device Name: AIRSTRIP OB
Manufacturer:
Device Classification Name: System, Monitoring, Perinatal
Regulation Number: HGM
Classification Product Code: 01/09/2009
Date Received: 01/23/2009
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: AIRSTRIP OB
Manufacturer:
Device Classification Name: System, Monitoring, Perinatal
Regulation Number: HGM
Classification Product Code: 01/09/2009
Date Received: 01/23/2009
Decision Date: Substantially Equivalent (SESE)
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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