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U.S. Department of Health and Human Services

510(k) Premarket Notification
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ProductCode: FOZ Applicant: NIPRO MEDICAL CORP. Decision Date To: 05/24/2024
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modification to: nipro safe touch safety fistula needle NIPRO MEDICAL CORP. K032777 11/14/2003
nipro bio-flex catheter NIPRO MEDICAL CORP. K022756 10/18/2002
nipro safelet cath NIPRO MEDICAL CORP. K013287 12/03/2001
nipro safetouch scalp vein and blood collection set NIPRO MEDICAL CORP. K011297 06/20/2001
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