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ULTRASTIM KIT

Page Type
Cleared 510(K)
510(k) Number
K013532
510(k) Type
Traditional
Applicant
AXELGAARD MFG. CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2002
Days to Decision
309 days
Submission Type
Statement

ULTRASTIM KIT

Page Type
Cleared 510(K)
510(k) Number
K013532
510(k) Type
Traditional
Applicant
AXELGAARD MFG. CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/2002
Days to Decision
309 days
Submission Type
Statement