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FDA 510(k), K992908, Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)
FDA 510(k), K992908, Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)
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510(K) Number: K992908
Device Name: Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)
Manufacturer: QUINTON, INC.
Device Classification Name: detector and alarm, arrhythmia
Regulation Number: 870.1025
Classification Product Code: DSI
Date Received: 08/30/1999
Decision Date: 03/06/2000
Regulation Medical Specialty: Cardiovascular
Device Name: Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)
Manufacturer: QUINTON, INC.
Device Classification Name: detector and alarm, arrhythmia
Regulation Number: 870.1025
Classification Product Code: DSI
Date Received: 08/30/1999
Decision Date: 03/06/2000
Regulation Medical Specialty: Cardiovascular
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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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