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FDA 510(k), K042557, INNOJECT AUTO-INJECTOR
FDA 510(k), K042557, INNOJECT AUTO-INJECTOR
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510(K) Number: K042557
Device Name: INNOJECT AUTO-INJECTOR
Manufacturer: INNOJECT, INC
Device Classification Name: introducer, syringe needle
Regulation Number: 880.6920
Classification Product Code: KZH
Date Received: 09/20/2004
Decision Date: 11/08/2004
Regulation Medical Specialty: General Hospital
Device Name: INNOJECT AUTO-INJECTOR
Manufacturer: INNOJECT, INC
Device Classification Name: introducer, syringe needle
Regulation Number: 880.6920
Classification Product Code: KZH
Date Received: 09/20/2004
Decision Date: 11/08/2004
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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