FDA 510(k), K201634, RG 3ml Medication Cartridge
FDA 510(k), K201634, RG 3ml Medication Cartridge
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510(K) Number: K201634
Device Name: RG 3ml Medication Cartridge
Manufacturer: Chengdu Shifeng Medical Technology Co., Ltd.
Device Classification Name: Accessories, Pump, Infusion
Regulation Number: 880.5725
Classification Product Code: MRZ
Date Received: 06/16/2020
Decision Date: 03/26/2021
Regulation Medical Specialty: General Hospital
Device Name: RG 3ml Medication Cartridge
Manufacturer: Chengdu Shifeng Medical Technology Co., Ltd.
Device Classification Name: Accessories, Pump, Infusion
Regulation Number: 880.5725
Classification Product Code: MRZ
Date Received: 06/16/2020
Decision Date: 03/26/2021
Regulation Medical Specialty: General Hospital
- 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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