Last synced on 30 November 2024 at 11:09 am

Device To Detect Antigens Of Biothreat Microbial Agents In Human Clinical Specimens

Page Type
Product Code
Definition
A device to detect antigens of biothreat microbial agents in human clinical specimens is identified as an in vitro diagnostic device intended for the detection of antigens of microbial agents in specimens collected from patients with signs and symptoms of infection with biothreat microbial agents and who have been exposed to these agents or are suspected or at risk of exposure.  Devices to detect antigens of biothreat microbial agents in human clinical specimens may be used for cadaver testing if the cadaver constitutes a source of human-to-human transmission and if testing is performed to prevent human disease.
Physical State
Membrane-bound antibodies in a plastic housing
Technical Method
Lateral flow chromatographic test
Target Area
Samples from the human body
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.4002
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 QID is linked to regulation 21CFR866.4002, which does not seem to exist yet. It may be pending at the moment.

Device To Detect Antigens Of Biothreat Microbial Agents In Human Clinical Specimens

Page Type
Product Code
Definition
A device to detect antigens of biothreat microbial agents in human clinical specimens is identified as an in vitro diagnostic device intended for the detection of antigens of microbial agents in specimens collected from patients with signs and symptoms of infection with biothreat microbial agents and who have been exposed to these agents or are suspected or at risk of exposure.  Devices to detect antigens of biothreat microbial agents in human clinical specimens may be used for cadaver testing if the cadaver constitutes a source of human-to-human transmission and if testing is performed to prevent human disease.
Physical State
Membrane-bound antibodies in a plastic housing
Technical Method
Lateral flow chromatographic test
Target Area
Samples from the human body
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.4002
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 QID is linked to regulation 21CFR866.4002, which does not seem to exist yet. It may be pending at the moment.