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FDA 510(k), K900260, AMBU LIFE KEY AND AMBU RES-CUE KEY
FDA 510(k), K900260, AMBU LIFE KEY AND AMBU RES-CUE KEY
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510(K) Number: K900260
Device Name: AMBU LIFE KEY AND AMBU RES-CUE KEY
Manufacturer: AMBU, INC.
Device Classification Name: ventilator, emergency, manual (resuscitator)
Regulation Number: 868.5915
Classification Product Code: BTM
Date Received: 01/17/1990
Decision Date: 06/08/1990
Regulation Medical Specialty: Anesthesiology
Device Name: AMBU LIFE KEY AND AMBU RES-CUE KEY
Manufacturer: AMBU, INC.
Device Classification Name: ventilator, emergency, manual (resuscitator)
Regulation Number: 868.5915
Classification Product Code: BTM
Date Received: 01/17/1990
Decision Date: 06/08/1990
Regulation Medical Specialty: Anesthesiology
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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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