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FDA 510(k), K915417, KOPAN'S TARGET
FDA 510(k), K915417, KOPAN'S TARGET
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510(K) Number: K915417
Device Name: KOPAN'S TARGET
Manufacturer: MEDICAL DEVICE TECHNOLOGIES, INC.
Device Classification Name: needle, aspiration and injection, disposable
Regulation Number: 878.4800
Classification Product Code: GAA
Date Received: 12/02/1991
Decision Date: 01/14/1992
Regulation Medical Specialty: General & Plastic Surgery
Device Name: KOPAN'S TARGET
Manufacturer: MEDICAL DEVICE TECHNOLOGIES, INC.
Device Classification Name: needle, aspiration and injection, disposable
Regulation Number: 878.4800
Classification Product Code: GAA
Date Received: 12/02/1991
Decision Date: 01/14/1992
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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