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TRI-LEVEL TDM CONTROL & I II III

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831500
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1983
Days to Decision
50 days

TRI-LEVEL TDM CONTROL & I II III

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831500
510(k) Type
Traditional
Applicant
ORTHO DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1983
Days to Decision
50 days