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Ivalon
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K946016
IVALON OPHTHALMIC SPONGE
March 22, 1995
K946015
IVALON EXTERNAL SPONGE
February 27, 1995
K913556
IVALON EMBOLIZATION PARTICLES
April 13, 1994