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GUIDOR(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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