FDA 510(k), K032425, INVISIJECT RESUSABLE AUTO-INJECTOR
FDA 510(k), K032425, INVISIJECT RESUSABLE AUTO-INJECTOR
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510(K) Number: K032425
Device Name: INVISIJECT RESUSABLE AUTO-INJECTOR
Manufacturer: BIOGEN
Device Classification Name: introducer, syringe needle
Regulation Number: 880.6920
Classification Product Code: KZH
Date Received: 08/06/2003
Decision Date: 11/05/2003
Regulation Medical Specialty: General Hospital
Device Name: INVISIJECT RESUSABLE AUTO-INJECTOR
Manufacturer: BIOGEN
Device Classification Name: introducer, syringe needle
Regulation Number: 880.6920
Classification Product Code: KZH
Date Received: 08/06/2003
Decision Date: 11/05/2003
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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