FDA 510(k), K902114, CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR
FDA 510(k), K902114, CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR
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
Total pages: 40
Fully redacted pages: 15
Content pages: 25
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