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FDA 510(k), K993120, MODIFIED BLOOD RECIPIENT SET
FDA 510(k), K993120, MODIFIED BLOOD RECIPIENT SET
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510(K) Number: K993120
Device Name: MODIFIED BLOOD RECIPIENT SET
Manufacturer: BAXTER HEALTHCARE CORP.
Device Classification Name: set, blood transfusion
Regulation Number: 880.5440
Classification Product Code: BRZ
Date Received: 09/20/1999
Decision Date: 11/17/1999
Regulation Medical Specialty: General Hospital
Device Name: MODIFIED BLOOD RECIPIENT SET
Manufacturer: BAXTER HEALTHCARE CORP.
Device Classification Name: set, blood transfusion
Regulation Number: 880.5440
Classification Product Code: BRZ
Date Received: 09/20/1999
Decision Date: 11/17/1999
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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