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C-REACTIVE PROTEIN (CRP):A LATEX SLIDE TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962019
510(k) Type
Traditional
Applicant
TECO DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1996
Days to Decision
186 days
Submission Type
Statement

C-REACTIVE PROTEIN (CRP):A LATEX SLIDE TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962019
510(k) Type
Traditional
Applicant
TECO DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1996
Days to Decision
186 days
Submission Type
Statement