Last synced on 20 December 2024 at 11:05 pm

System For Detection Of Nucleic Acid From Non-Viral Microorganism(S) Causing Stis Using Specimens Collected At Home

Page Type
Product Code
Definition
This device is an in vitro diagnostic system intended for self-collecting specimens in home settings or similar environments and testing in a clinical laboratory for detection of nucleic acids from non-viral microorganism(s) causing sexually transmitted infections. The device is intended to aid in the diagnosis of sexually transmitted infections. The device is intended for prescription use or over-the-counter use.
Physical State
In vitro diagnostic test system consisting of home collection kit and reagents and associated instrumentation for the detection of nucleic acid sequences from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) in home collected specimens.
Technical Method
In vitro diagnostic test system that detects and identifies nucleic acid sequences from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) in home collected specimens.
Target Area
Home collected urogenital specimens from users suspected of Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) infection.
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3385
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 QYA is linked to regulation 21CFR866.3385, which does not seem to exist yet. It may be pending at the moment.

System For Detection Of Nucleic Acid From Non-Viral Microorganism(S) Causing Stis Using Specimens Collected At Home

Page Type
Product Code
Definition
This device is an in vitro diagnostic system intended for self-collecting specimens in home settings or similar environments and testing in a clinical laboratory for detection of nucleic acids from non-viral microorganism(s) causing sexually transmitted infections. The device is intended to aid in the diagnosis of sexually transmitted infections. The device is intended for prescription use or over-the-counter use.
Physical State
In vitro diagnostic test system consisting of home collection kit and reagents and associated instrumentation for the detection of nucleic acid sequences from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) in home collected specimens.
Technical Method
In vitro diagnostic test system that detects and identifies nucleic acid sequences from Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) in home collected specimens.
Target Area
Home collected urogenital specimens from users suspected of Chlamydia trachomatis (CT) and/or Neisseria gonorrhoeae (GC) infection.
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3385
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 QYA is linked to regulation 21CFR866.3385, which does not seem to exist yet. It may be pending at the moment.