Last synced on 18 April 2025 at 11:05 pm

Test For Detection Of Microorganism(S) Causing Sexually Transmitted Infections Performed By Lay Users

Page Type
Product Code
Definition
This device is an in vitro diagnostic device for the detection and/or differentiation of nucleic acids from non-viral microorganism(s) causing sexually transmitted infections in clinical specimens for use in home settings, or similar environments. The test is intended for prescription or over-the-counter use.
Physical State
In vitro diagnostic device consisting of reagents and associated instrumentation for the detection of nucleic acid sequences from sexually transmitted non-viral microorganism(s).
Technical Method
In vitro diagnostic self-testing device that detects and identifies nucleic acid sequences from sexually transmitted non-viral microorganism(s).
Target Area
Clinical specimens from patients suspected of from sexually transmitted non-viral microorganism(s).
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3386
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 SEA is linked to regulation 21CFR866.3386, which does not seem to exist yet. It may be pending at the moment.

Test For Detection Of Microorganism(S) Causing Sexually Transmitted Infections Performed By Lay Users

Page Type
Product Code
Definition
This device is an in vitro diagnostic device for the detection and/or differentiation of nucleic acids from non-viral microorganism(s) causing sexually transmitted infections in clinical specimens for use in home settings, or similar environments. The test is intended for prescription or over-the-counter use.
Physical State
In vitro diagnostic device consisting of reagents and associated instrumentation for the detection of nucleic acid sequences from sexually transmitted non-viral microorganism(s).
Technical Method
In vitro diagnostic self-testing device that detects and identifies nucleic acid sequences from sexually transmitted non-viral microorganism(s).
Target Area
Clinical specimens from patients suspected of from sexually transmitted non-viral microorganism(s).
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3386
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 SEA is linked to regulation 21CFR866.3386, which does not seem to exist yet. It may be pending at the moment.