Product Classification

• Device: dna probe, nucleic acid amplification, chlamydia
• Regulation Description: Chlamydia serological reagents.
• Regulation Medical Specialty: Microbiology
• Review Panel: Microbiology
• Product Code: MKZ
• Premarket Review: Division of Microbiology Devices (DMD); Division of Microbiology Devices (DMD)
• Submission Type: 510(k)
• Regulation Number: 866.3120
• Device Class: 1
• Total Product Life Cycle (TPLC): TPLC Product Code Report
• GMP Exempt?: No
• Summary Malfunction Reporting: Ineligible
• Implanted Device?: No
• Life-Sustain/Support Device?: No

Recognized Consensus Standard

• 7-260 CLSI MM03-3rd Edition (Replaces MM03-A2)
  Molecular Diagnostic Methods for Infectious Diseases; Approved Guideline

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