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FDA 510(k), K971782, BONE AND MARROW COLLECTION SYSTEM KIT
FDA 510(k), K971782, BONE AND MARROW COLLECTION SYSTEM KIT
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510(K) Number: K971782
Device Name: BONE AND MARROW COLLECTION SYSTEM KIT
Manufacturer: BIOMEDICAL ENT., INC.
Device Classification Name: motor, surgical instrument, ac-powered
Regulation Number: 878.4820
Classification Product Code: GEY
Date Received: 05/14/1997
Decision Date: 07/29/1997
Regulation Medical Specialty: General & Plastic Surgery
Device Name: BONE AND MARROW COLLECTION SYSTEM KIT
Manufacturer: BIOMEDICAL ENT., INC.
Device Classification Name: motor, surgical instrument, ac-powered
Regulation Number: 878.4820
Classification Product Code: GEY
Date Received: 05/14/1997
Decision Date: 07/29/1997
Regulation Medical Specialty: General & Plastic Surgery
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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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