Antisera, Cf, Herpesvirus Hominis 1,2

Device Code: 3256

Product Code(s): GQO

Device Classification Information

• Device Type ID: 3256
• Device Name: Antisera, Cf, Herpesvirus Hominis 1,2
• Regulation Description: Herpes Simplex Virus Serological Assays.
• Regulation Medical Specialty: Microbiology
• Review Panel: Microbiology
• Premarket Review: Office Of In Vitro Diagnostics And Radiological Health (OIR)
• Submission Type: 510(k)
• CFR Regulation Number: 866.3305 [🔎]
• FDA Device Classification: Class 2 Medical Device
• Product Code: GQO
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: No
• Life Support Device: No
• Third Party Review: Not Third Party Eligible

Recognized Standards

Total Product Life Cycle

• Device Type ID: 3256
• Device: Antisera, Cf, Herpesvirus Hominis 1,2
• Product Code: GQO
• FDA Device Classification: Class 2 Medical Device
• Regulation Description: Herpes Simplex Virus Serological Assays.
• CFR Regulation Number: 866.3305 [🔎]

TPLC Last Update: 2019-04-02 20:26:32