Last synced on 20 December 2024 at 11:05 pm

Non-Variola Orthopoxvirus Real-Time Pcr Primer And Probe Set

Page Type
Product Code
Definition
In vitro qualitative detection of non-variola Orthopoxvirus nucleic acids extracted from human specimens or viral culture.
Physical State
Provided in the device are Non-variola Orthopoxvirus Real-time PCR Assay Reagents which include primers and probes, positive controls, and an extraction control.
Technical Method
A Non-variola Orthopoxvirus Real-time PCR Assay method which includes nucleic acid isolation, amplification and detection of nucleic acid using a PCR instrument. A set of primers and probes are used for the in vitro detection of non-variola Orthopoxvirus nucleic acids extracted from human specimens or viral culture.
Target Area
Human Clinical Samples (e.g., pustular or vesicular rash specimens) and viral cell culture lysates
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3315
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code PBK is linked to regulation 21CFR866.3315, which does not seem to exist yet. It may be pending at the moment.

Non-Variola Orthopoxvirus Real-Time Pcr Primer And Probe Set

Page Type
Product Code
Definition
In vitro qualitative detection of non-variola Orthopoxvirus nucleic acids extracted from human specimens or viral culture.
Physical State
Provided in the device are Non-variola Orthopoxvirus Real-time PCR Assay Reagents which include primers and probes, positive controls, and an extraction control.
Technical Method
A Non-variola Orthopoxvirus Real-time PCR Assay method which includes nucleic acid isolation, amplification and detection of nucleic acid using a PCR instrument. A set of primers and probes are used for the in vitro detection of non-variola Orthopoxvirus nucleic acids extracted from human specimens or viral culture.
Target Area
Human Clinical Samples (e.g., pustular or vesicular rash specimens) and viral cell culture lysates
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3315
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code PBK is linked to regulation 21CFR866.3315, which does not seem to exist yet. It may be pending at the moment.