Product Classification

• Device: ß-glucocerebrosidase (gba) newborn screening test system
• Definition: For quantitative measurement of the activity of ß-glucocerebrosidase (GBA) from newborn dried blood spot specimens.
• Physical State: Neonatal screening test
• Technical Method: Quantitative fluorimetric enzymatic activity assay.
• Target Area: Newborn dried blood spot specimens.
• Regulation Medical Specialty: Clinical Chemistry
• Review Panel: Clinical Chemistry
• Product Code: PQV
• Premarket Review: Office of In Vitro Diagnostics (OHT7); Division of Chemistry and Toxicology Devices (DCTD)
• Submission Type: 510(k)
• Regulation Number: 862.1488
• Device Class: 2
• Total Product Life Cycle (TPLC): TPLC Product Code Report
• GMP Exempt?: No
• Summary Malfunction Reporting: Ineligible
• 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