FDA 510(k), K022236, RECOVERY FILTER SYSTEM, MODEL RF-048F
FDA 510(k), K022236, RECOVERY FILTER SYSTEM, MODEL RF-048F
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510(K) Number: K022236
Device Name: RECOVERY FILTER SYSTEM, MODEL RF-048F
Manufacturer: C.R. BARD, INC.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 07/11/2002
Decision Date: 11/27/2002
Regulation Medical Specialty: Cardiovascular
Device Name: RECOVERY FILTER SYSTEM, MODEL RF-048F
Manufacturer: C.R. BARD, INC.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 07/11/2002
Decision Date: 11/27/2002
Regulation Medical Specialty: Cardiovascular
- 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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