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ALOKA PROUSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K110207
510(k) Type
Traditional
Applicant
ALOKA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2011
Days to Decision
23 days
Submission Type
Summary

ALOKA PROUSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K110207
510(k) Type
Traditional
Applicant
ALOKA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2011
Days to Decision
23 days
Submission Type
Summary