Last synced on 20 December 2024 at 11:05 pm

Device To Detect Microbial Colonization Directly From Clinical Specimens.

Page Type
Product Code
Definition
A device to detect microbial colonization directly from clinical specimens is a qualitative in vitro diagnostic device intended for the detection and identification of microbial-associated targets from patients who are suspected of being colonized with a microbial pathogen and may present a risk of transmission to other patients and health care workers. This device is intended to aid in the detection of microbial colonizers for the prevention and control of infection in healthcare settings when used in conjunction with clinical and laboratory findings.
Physical State
Single-use assay with reagents and disposables and associated instrument system
Technical Method
Qualitative nucleic acid test
Target Area
Clinical specimens
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3967
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 SBT is linked to regulation 21CFR866.3967, which does not seem to exist yet. It may be pending at the moment.

Device To Detect Microbial Colonization Directly From Clinical Specimens.

Page Type
Product Code
Definition
A device to detect microbial colonization directly from clinical specimens is a qualitative in vitro diagnostic device intended for the detection and identification of microbial-associated targets from patients who are suspected of being colonized with a microbial pathogen and may present a risk of transmission to other patients and health care workers. This device is intended to aid in the detection of microbial colonizers for the prevention and control of infection in healthcare settings when used in conjunction with clinical and laboratory findings.
Physical State
Single-use assay with reagents and disposables and associated instrument system
Technical Method
Qualitative nucleic acid test
Target Area
Clinical specimens
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3967
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 SBT is linked to regulation 21CFR866.3967, which does not seem to exist yet. It may be pending at the moment.