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
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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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