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C-REACTIVE PROTEIN (CRP) AGGLUTINATION LATEX KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962049
510(k) Type
Traditional
Applicant
POLYMEDCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1996
Days to Decision
204 days
Submission Type
Statement

C-REACTIVE PROTEIN (CRP) AGGLUTINATION LATEX KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962049
510(k) Type
Traditional
Applicant
POLYMEDCO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1996
Days to Decision
204 days
Submission Type
Statement