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S.H.P. Intl. Pty., Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K014273
ACUSTIM
June 12, 2002
K954334
ACUPLUS
January 22, 1996