FDA 510(k) Applications Submitted by OMI MANUFACTURING PTY., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K060971 04/07/2006 OMI RETRACTABLE SAFTEY SYRINGE, VARIOUS OMI MANUFACTURING PTY., LTD.
K032242 07/21/2003 PERSONNA PLUS SAFETY SCALPEL SYSTEM OMI MANUFACTURING PTY., LTD.


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