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RHEUMA-LEX(TM) SYST: RHEUMATOID FACTOR LATEX TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915320
510(k) Type
Traditional
Applicant
TRINITY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/1992
Days to Decision
381 days
Submission Type
Statement

RHEUMA-LEX(TM) SYST: RHEUMATOID FACTOR LATEX TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915320
510(k) Type
Traditional
Applicant
TRINITY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/1992
Days to Decision
381 days
Submission Type
Statement