Product Classification

• Device: device, germicidal, ultraviolet
• Regulation Description: Medical ultraviolet air purifier.
• Regulation Medical Specialty: General Hospital
• Review Panel: General Hospital
• Product Code: MKB
• Submission Type: 510(k)
• Regulation Number: 880.6500
• Device Class: 2
• Total Product Life Cycle (TPLC): TPLC Product Code Report
• GMP Exempt?: No

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.