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PENRITH ELETTRA ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100598
510(k) Type
Traditional
Applicant
PENRITH CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2010
Days to Decision
261 days
Submission Type
Summary

PENRITH ELETTRA ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K100598
510(k) Type
Traditional
Applicant
PENRITH CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2010
Days to Decision
261 days
Submission Type
Summary