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LYPHOCHEK TUMOR MARKER CONTROLS, LEVELS I AND II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891680
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1989
Days to Decision
84 days

LYPHOCHEK TUMOR MARKER CONTROLS, LEVELS I AND II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K891680
510(k) Type
Traditional
Applicant
BIO-RAD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/1989
Days to Decision
84 days