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GUIDOR(TM)

Page Type
Cleared 510(K)
510(k) Number
K912724
510(k) Type
Traditional
Applicant
PROCORDIA ORATECH AB
Country
Sweden
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/13/1993
Days to Decision
695 days
Submission Type
Statement

GUIDOR(TM)

Page Type
Cleared 510(K)
510(k) Number
K912724
510(k) Type
Traditional
Applicant
PROCORDIA ORATECH AB
Country
Sweden
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/13/1993
Days to Decision
695 days
Submission Type
Statement