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CROMATEST RHEUMATOID DIAGNOSTIC/RF LATEX TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904498
510(k) Type
Traditional
Applicant
BIOTRAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1990
Days to Decision
27 days

CROMATEST RHEUMATOID DIAGNOSTIC/RF LATEX TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K904498
510(k) Type
Traditional
Applicant
BIOTRAX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1990
Days to Decision
27 days