Last synced on 20 December 2024 at 11:05 pm

Multiplex Nucleic Acid Detection System For Biothreat Agents

Page Type
Product Code
Definition
A multiplex nucleic acid detection system for biothreat agents is a qualitative in vitro diagnostic test for detection and identification of nucleic acids from biothreat pathogens in human clinical specimens
Physical State
Multiplex nucleic acid detection systems are in vitro diagnostic devices that include reagents and associated instrumentation for detection and identification of biothreat nucleic acids from human clinical specimens
Technical Method
A qualitative in vitro diagnostic assay that detects and identifies nucleic acids from multiple biothreat pathogens
Target Area
Whole blood specimens
Regulation Medical Specialty
Immunology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.4000
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 QVR is linked to regulation 21CFR866.4000, which does not seem to exist yet. It may be pending at the moment.

Multiplex Nucleic Acid Detection System For Biothreat Agents

Page Type
Product Code
Definition
A multiplex nucleic acid detection system for biothreat agents is a qualitative in vitro diagnostic test for detection and identification of nucleic acids from biothreat pathogens in human clinical specimens
Physical State
Multiplex nucleic acid detection systems are in vitro diagnostic devices that include reagents and associated instrumentation for detection and identification of biothreat nucleic acids from human clinical specimens
Technical Method
A qualitative in vitro diagnostic assay that detects and identifies nucleic acids from multiple biothreat pathogens
Target Area
Whole blood specimens
Regulation Medical Specialty
Immunology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.4000
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 QVR is linked to regulation 21CFR866.4000, which does not seem to exist yet. It may be pending at the moment.