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ULTROID HEMORRHOID MANAGEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K023706
510(k) Type
Traditional
Applicant
ULTROID, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2003
Days to Decision
71 days
Submission Type
Statement

ULTROID HEMORRHOID MANAGEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K023706
510(k) Type
Traditional
Applicant
ULTROID, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2003
Days to Decision
71 days
Submission Type
Statement