Last synced on 13 June 2025 at 11:06 pm

CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972160
510(k) Type
Traditional
Applicant
TRINITY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1997
Days to Decision
53 days
Submission Type
Statement

CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972160
510(k) Type
Traditional
Applicant
TRINITY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1997
Days to Decision
53 days
Submission Type
Statement