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FDA 510(k), K171237, FMS VUE II Fluid Management and Tissue Debridement System
FDA 510(k), K171237, FMS VUE II Fluid Management and Tissue Debridement System
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510(K) Number: K171237
Device Name: FMS VUE II Fluid Management and Tissue Debridement System
Manufacturer: Medos International SARL
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 04/27/2017
Decision Date: 01/18/2018
Regulation Medical Specialty: Orthopedic
Device Name: FMS VUE II Fluid Management and Tissue Debridement System
Manufacturer: Medos International SARL
Device Classification Name: Arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 04/27/2017
Decision Date: 01/18/2018
Regulation Medical Specialty: Orthopedic
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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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