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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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