FDA 510(k) Applications Submitted by RD MEDICAL MFG., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K010538 02/23/2001 PARSET NEEDLELESS PRIMARY SET FOR BLUNT CANNULA, A10003E, PARSET NEEDLELESS SECONDARY SET WITH BLUNT CANNULA, A14003E RD MEDICAL MFG., INC.
K001102 04/05/2000 PARSET PRIMARY SET WITH CHECK VALVE, MODEL A10002E RD MEDICAL MFG., INC.
K992104 06/22/1999 PARSET, MODEL A10001E RD MEDICAL MFG., INC.
K000017 01/03/2000 PARSET SECONDARY ADMINISTRATION SET, LUERLOCK, MODEL A14001E, PARSET SECONDARY SECONDARY ADMINISTRATION SET, MODEL A1400 RD MEDICAL MFG., INC.


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