Product Classification

• Device: system, test, genotypic detection, resistant markers, staphylococcus colonies
• Regulation Description: Antimicrobial susceptibility test powder.
• Regulation Medical Specialty: Microbiology
• Review Panel: Microbiology
• Product Code: MYI
• Premarket Review: Office of In Vitro Diagnostics (OHT7); Division of Microbiology Devices (DMD)
• Submission Type: 510(k)
• Regulation Number: 866.1640
• 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

• center for measurement standards of industrial
• global quality and regulatory services
• regulatory technology services, llc