FDA 510(k) Applications Submitted by MANI, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K050150 01/24/2005 MANI NEEDLE & SUTURE PACK MANI, INC.
K053636 12/29/2005 MANI NEEDLE & SUTURE PACK (PGA ABSORBABLE) MANI, INC.
K053637 12/29/2005 MANI NEEDLE & SUTURE PACK (NYLON) MANI, INC.
K053638 12/29/2005 MANI NEEDLE & SUTURE PACK (SILK) MANI, INC.


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