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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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