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FDA 510(k), K051667, EZ-JECT
FDA 510(k), K051667, EZ-JECT
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510(K) Number: K051667
Device Name: EZ-JECT
Manufacturer: GEORGE J HATTUB
Device Classification Name: Introducer, Syringe Needle
Regulation Number: KZH
Classification Product Code: 06/22/2005
Date Received: 09/27/2005
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: EZ-JECT
Manufacturer: GEORGE J HATTUB
Device Classification Name: Introducer, Syringe Needle
Regulation Number: KZH
Classification Product Code: 06/22/2005
Date Received: 09/27/2005
Decision Date: Substantially Equivalent (SESE)
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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