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RHEUMATOID FACTOR LATEX-ENHANCED IMMUNOTURBIDIMETRIC TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972220
510(k) Type
Traditional
Applicant
RANDOX LABORATORIES, LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
9/9/1997
Days to Decision
89 days
Submission Type
Statement

RHEUMATOID FACTOR LATEX-ENHANCED IMMUNOTURBIDIMETRIC TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972220
510(k) Type
Traditional
Applicant
RANDOX LABORATORIES, LTD.
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
9/9/1997
Days to Decision
89 days
Submission Type
Statement