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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 5 of 5 Results
ProductCode: KNW Applicant: PROMEX, INC. Decision Date To: 04/25/2024
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vacuum assisted core biopsy device PROMEX, INC. K010400 07/24/2001
bone biopsy needle PROMEX, INC. K001132 05/01/2000
automated core biopsy device PROMEX, INC. K994272 01/07/2000
manual bone marrow biopsy device PROMEX, INC. K993435 12/06/1999
trocar style needle/co-axial introducer needle PROMEX, INC. K954265 09/29/1995
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