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FDA 510(k), K922117, C-TRAK BIOPSY SYSTEM
FDA 510(k), K922117, C-TRAK BIOPSY SYSTEM
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510(K) Number: K922117
Device Name: C-TRAK BIOPSY SYSTEM
Manufacturer: CARE WISE MEDICAL PRODUCTS CORP.
Device Classification Name: probe, uptake, nuclear
Regulation Number: 892.1320
Classification Product Code: IZD
Date Received: 05/05/1992
Decision Date: 10/14/1992
Regulation Medical Specialty: Radiology
Device Name: C-TRAK BIOPSY SYSTEM
Manufacturer: CARE WISE MEDICAL PRODUCTS CORP.
Device Classification Name: probe, uptake, nuclear
Regulation Number: 892.1320
Classification Product Code: IZD
Date Received: 05/05/1992
Decision Date: 10/14/1992
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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