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FDA 510(k), K003576, Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503
FDA 510(k), K003576, Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503
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510(K) Number: K003576
Device Name: Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503
Manufacturer: QUINTON, INC.
Device Classification Name: detector and alarm, arrhythmia
Regulation Number: 870.1025
Classification Product Code: DSI
Date Received: 11/20/2000
Decision Date: 01/25/2001
Regulation Medical Specialty: Cardiovascular
Device Name: Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503
Manufacturer: QUINTON, INC.
Device Classification Name: detector and alarm, arrhythmia
Regulation Number: 870.1025
Classification Product Code: DSI
Date Received: 11/20/2000
Decision Date: 01/25/2001
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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