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FDA 510(k), K962319, NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES
FDA 510(k), K962319, NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES
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510(K) Number: K962319
Device Name: NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES
Manufacturer: NEOPROBE CORP.
Device Classification Name: probe, uptake, nuclear
Regulation Number: 892.1320
Classification Product Code: IZD
Date Received: 06/17/1996
Decision Date: 09/13/1996
Regulation Medical Specialty: Radiology
Device Name: NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES
Manufacturer: NEOPROBE CORP.
Device Classification Name: probe, uptake, nuclear
Regulation Number: 892.1320
Classification Product Code: IZD
Date Received: 06/17/1996
Decision Date: 09/13/1996
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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