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
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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