FDA 510(k), K963597, SILENT NIGHT I
FDA 510(k), K963597, SILENT NIGHT I
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510(K) Number: K963597
Device Name: SILENT NIGHT I
Manufacturer:
Device Classification Name: Ventilatory Effort Recorder
Regulation Number: 868.2375
Classification Product Code: MNR
Date Received: 09/09/1996
Decision Date: 01/23/1997
Regulation Medical Specialty: Anesthesiology
Device Name: SILENT NIGHT I
Manufacturer:
Device Classification Name: Ventilatory Effort Recorder
Regulation Number: 868.2375
Classification Product Code: MNR
Date Received: 09/09/1996
Decision Date: 01/23/1997
Regulation Medical Specialty: Anesthesiology