Product Classification

• Device: direct agglutination test, toxoplasma gondii
• Regulation Description: Toxoplasma gondiiserological reagents.
• Regulation Medical Specialty: Microbiology
• Review Panel: Microbiology
• Product Code: LLA
• Submission Type: 510(k)
• Regulation Number: 866.3780
• Device Class: 2
• Total Product Life Cycle (TPLC): TPLC Product Code Report
• GMP Exempt?: No

Recognized Consensus Standard

• CLSI M36-A Clinical Use and Interpretation of Serologic Tests for Toxoplasma gondii

Third Party Review

• Eligible for Accredited Persons Expansion Pilot Program

Accredited Persons

• dekra certification b.v.
• intertek testing services
• regulatory technology services, llc
• tuv sud america inc.
• underwriters laboratories, inc.