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FDA 510(k), K150893, IntelliCuff
FDA 510(k), K150893, IntelliCuff
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$89.00 USD
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510(K) Number: K150893
Device Name: IntelliCuff
Manufacturer: STEFFEN BODEN
Device Classification Name: Cuff, Tracheal Tube, Inflatable
Regulation Number: BSK
Classification Product Code: KXA
Date Received: 04/02/2015
Decision Date: 01/29/2016
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
Device Name: IntelliCuff
Manufacturer: STEFFEN BODEN
Device Classification Name: Cuff, Tracheal Tube, Inflatable
Regulation Number: BSK
Classification Product Code: KXA
Date Received: 04/02/2015
Decision Date: 01/29/2016
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Anesthesiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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