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DIAMEDIX IS-RUBELLA IGM CAPTURE TEST SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001875
510(k) Type
Traditional
Applicant
DIAMEDIX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2000
Days to Decision
62 days
Submission Type
Summary

DIAMEDIX IS-RUBELLA IGM CAPTURE TEST SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001875
510(k) Type
Traditional
Applicant
DIAMEDIX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2000
Days to Decision
62 days
Submission Type
Summary