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FDA 510(k), K961321, GAMMA GUIDANCE SYSTEM
FDA 510(k), K961321, GAMMA GUIDANCE SYSTEM
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510(K) Number: K961321
Device Name: GAMMA GUIDANCE SYSTEM
Manufacturer: RADIATION MONITORING DEVICES, INC.
Device Classification Name: Probe, Uptake, Nuclear
Regulation Number: 892.1320
Classification Product Code: IZD
Date Received: 04/05/1996
Decision Date: 02/10/1997
Regulation Medical Specialty: Radiology
Device Name: GAMMA GUIDANCE SYSTEM
Manufacturer: RADIATION MONITORING DEVICES, INC.
Device Classification Name: Probe, Uptake, Nuclear
Regulation Number: 892.1320
Classification Product Code: IZD
Date Received: 04/05/1996
Decision Date: 02/10/1997
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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