Product Classification

• Device: anti-glutamate receptor (type nmda) ifa
• Regulation Description: Multiple autoantibodies immunological test system.
• Definition: Intended for the qualitative determination of autoantibodies against glutamate receptor (type NMDA) in human serum. Used as an aid in the diagnosis of anti-glutamate receptor (type NMDA) autoimmune encephalitis in conjunction with other laboratory and clinical findings.
• Physical State: Solid, liquid
• Technical Method: Immunofluorescent assay with multiple substrates
• Target Area: Human serum
• Regulation Medical Specialty: Immunology
• Review Panel: Immunology
• Product Code: OSK
• Premarket Review: Office of In Vitro Diagnostics (OHT7); Division of Immunology and Hematology Devices (DIHD)
• Submission Type: 510(k)
• Regulation Number: 866.5660
• Device Class: 2
• Total Product Life Cycle (TPLC): TPLC Product Code Report
• GMP Exempt?: No
• Summary Malfunction Reporting: Eligible
• Implanted Device?: No
• Life-Sustain/Support Device?: No

Third Party Review

• Eligible for 510(k) Third Party Review Program

Accredited Persons

• global quality and regulatory services
• regulatory technology services, llc