Last synced on 14 November 2025 at 11:06 pm

C-REACTIVE PROTEIN (CRP) AGGLUTINATION LATEX KIT

Page Type
Cleared 510(K)
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)
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