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PROULTRA PIEZO ULTRASONIC

Page Type
Cleared 510(K)
510(k) Number
K113430
510(k) Type
Traditional
Applicant
SATELEC-ACTEON GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2012
Days to Decision
94 days
Submission Type
Statement

PROULTRA PIEZO ULTRASONIC

Page Type
Cleared 510(K)
510(k) Number
K113430
510(k) Type
Traditional
Applicant
SATELEC-ACTEON GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2012
Days to Decision
94 days
Submission Type
Statement