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THE DDI SERODOT RUBELLA IGG TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K875368
510(k) Type
Traditional
Applicant
DISEASE DETECTION INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1988
Days to Decision
83 days

THE DDI SERODOT RUBELLA IGG TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K875368
510(k) Type
Traditional
Applicant
DISEASE DETECTION INTERNATIONAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1988
Days to Decision
83 days