Last synced on 20 December 2024 at 11:05 pm

Hsv-1 And Hsv-2 Cns Nucleic-Acid Based Panel

Page Type
Product Code
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
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3307
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
Yes
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code PGH is linked to regulation 21CFR866.3307, which does not seem to exist yet. It may be pending at the moment.

Hsv-1 And Hsv-2 Cns Nucleic-Acid Based Panel

Page Type
Product Code
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
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3307
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
Yes
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code PGH is linked to regulation 21CFR866.3307, which does not seem to exist yet. It may be pending at the moment.