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Sonokinetics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K990572
SONOTOME
May 21, 1999
K930629
ACRYL-X II SYSTEM
January 21, 1994
K911548
ACRYL-X SYSTEM TM
June 28, 1991