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FDA 510(k), K940025, MANAN BONE MARROW HARVEST NEEDLES
FDA 510(k), K940025, MANAN BONE MARROW HARVEST NEEDLES
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510(K) Number: K940025
Device Name: MANAN BONE MARROW HARVEST NEEDLES
Manufacturer: MANAN MEDICAL PRODUCTS, INC.
Device Classification Name: Needle, Aspiration And Injection, Disposable
Regulation Number: 878.4800
Classification Product Code: GAA
Date Received: 01/03/1994
Decision Date: 02/25/1994
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MANAN BONE MARROW HARVEST NEEDLES
Manufacturer: MANAN MEDICAL PRODUCTS, INC.
Device Classification Name: Needle, Aspiration And Injection, Disposable
Regulation Number: 878.4800
Classification Product Code: GAA
Date Received: 01/03/1994
Decision Date: 02/25/1994
Regulation Medical Specialty: General & Plastic Surgery
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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