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FDA 510(k), K020530, EVANS SUB-Q, MODEL MC4206
FDA 510(k), K020530, EVANS SUB-Q, MODEL MC4206
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510(K) Number: K020530
Device Name: EVANS SUB-Q, MODEL MC4206
Manufacturer: EVANS MEDICAL, INC.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 02/19/2002
Decision Date: 04/29/2002
Regulation Medical Specialty: General Hospital
Device Name: EVANS SUB-Q, MODEL MC4206
Manufacturer: EVANS MEDICAL, INC.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 02/19/2002
Decision Date: 04/29/2002
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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