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ORTHODONTICARTIDE

Page Type
Cleared 510(K)
510(k) Number
K800458
510(k) Type
Traditional
Applicant
EUROPEAN ORTHODONTIC PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1980
Days to Decision
25 days

ORTHODONTICARTIDE

Page Type
Cleared 510(K)
510(k) Number
K800458
510(k) Type
Traditional
Applicant
EUROPEAN ORTHODONTIC PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1980
Days to Decision
25 days