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FDA 510(k), K121270, BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM
FDA 510(k), K121270, BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM
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510(K) Number: K121270
Device Name: BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM
Manufacturer: BIOJECT MEDICAL TECHNOLOGIES INC.
Device Classification Name: Injector, Fluid, Non-Electrically Powered
Regulation Number: 880.5430
Classification Product Code: KZE
Date Received: 04/26/2012
Decision Date: 07/19/2012
Regulation Medical Specialty: General Hospital
Device Name: BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM
Manufacturer: BIOJECT MEDICAL TECHNOLOGIES INC.
Device Classification Name: Injector, Fluid, Non-Electrically Powered
Regulation Number: 880.5430
Classification Product Code: KZE
Date Received: 04/26/2012
Decision Date: 07/19/2012
Regulation Medical Specialty: General Hospital
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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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