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FDA 510(k), K001582, LIBERTY 9000 BREAST COIL WITH DISPOSABLE BIOPSY PLATE
FDA 510(k), K001582, LIBERTY 9000 BREAST COIL WITH DISPOSABLE BIOPSY PLATE
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510(K) Number: K001582
Device Name: LIBERTY 9000 BREAST COIL WITH DISPOSABLE BIOPSY PLATE
Manufacturer: USA INSTRUMENTS, INC.
Device Classification Name: coil, magnetic resonance, specialty
Regulation Number: 892.1000
Classification Product Code: MOS
Date Received: 05/22/2000
Decision Date: 07/17/2000
Regulation Medical Specialty: Radiology
Device Name: LIBERTY 9000 BREAST COIL WITH DISPOSABLE BIOPSY PLATE
Manufacturer: USA INSTRUMENTS, INC.
Device Classification Name: coil, magnetic resonance, specialty
Regulation Number: 892.1000
Classification Product Code: MOS
Date Received: 05/22/2000
Decision Date: 07/17/2000
Regulation Medical Specialty: Radiology
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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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