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F-SERIES IMPLANT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850706
510(k) Type
Traditional
Applicant
OMNI INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1985
Days to Decision
47 days

F-SERIES IMPLANT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850706
510(k) Type
Traditional
Applicant
OMNI INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1985
Days to Decision
47 days