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FDA 510(k), K033916, GRI-BAG, GRI-BAG AP
FDA 510(k), K033916, GRI-BAG, GRI-BAG AP
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$149.00 USD
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510(K) Number: K033916
Device Name: GRI-BAG, GRI-BAG AP
Manufacturer: LABORATORIOS GRIFOLS, S.A.
Device Classification Name: container, i.v.
Regulation Number: 880.5025
Classification Product Code: KPE
Date Received: 12/18/2003
Decision Date: 12/30/2003
Regulation Medical Specialty: General Hospital
Device Name: GRI-BAG, GRI-BAG AP
Manufacturer: LABORATORIOS GRIFOLS, S.A.
Device Classification Name: container, i.v.
Regulation Number: 880.5025
Classification Product Code: KPE
Date Received: 12/18/2003
Decision Date: 12/30/2003
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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