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U.S. Department of Health and Human Services

Product Classification
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Device hsv-1 and hsv-2 cns nucleic-acid based panel
Definition Intended for the qualitative detection and differentiation of HSV-1 and HSV-2 in cerebrospinal fluid (CSF) from patients with signs and symptoms of Herpes Simplex Virus (HSV) central nervous system (CNS) infection. This test is an aid in the diagnosis of HSV-1 and HSV-2 CNS infections in conjunction with other clinical and laboratory findings. Negative results do not preclude HSV-1 or HSV-2 infection and should not be used as the sole basis for treatment or other patient management decisions.
Physical State Reagent Assay Kit and Instrument
Technical Method Real-time Polymerase Chain Reaction Assay
Target Area Not Applicable, the device is an In vitro diagnostic device
Regulation Medical Specialty Microbiology
Review Panel Microbiology
Product CodePGH
Premarket Review Office of In Vitro Diagnostics (OHT7)
Division of Microbiology Devices (DMD)
Submission Type 510(k)
Regulation Number 866.3307
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? Yes
Third Party Review Not Third Party Eligible
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