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FDA 510(k), K902114, CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR
FDA 510(k), K902114, CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR
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510(K) Number: K902114
Device Name: CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR
Manufacturer: DIEMOLDING CORP.
Device Classification Name: cuff, tracheal tube, inflatable
Regulation Number: 868.5750
Classification Product Code: BSK
Date Received: 05/11/1990
Decision Date: 07/18/1990
Regulation Medical Specialty: Anesthesiology
Device Name: CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR
Manufacturer: DIEMOLDING CORP.
Device Classification Name: cuff, tracheal tube, inflatable
Regulation Number: 868.5750
Classification Product Code: BSK
Date Received: 05/11/1990
Decision Date: 07/18/1990
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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