Last synced on 20 December 2024 at 11:05 pm

Test For Detection Of Antibodies Associated With Syphilis Performed By Lay Users

Page Type
Product Code
Definition
Test for detection of antibodies associated with syphilis performed by lay users is an in vitro diagnostic device used for detection of antibodies in clinical specimens for use in home settings, or similar environments. The device is intended to aid in diagnosis of syphilis and intended for prescription use or over-the-counter use.
Physical State
Plastic cassette containing nitrocellulose membrane embedded with reagents capable of identifying analyte-specific antibodies in a blood sample.
Technical Method
Immobilization and visualization of antibodies specific to Syphilis disease using lateral flow technology.
Target Area
Blood drop exposed on the fingertip via fingerstick puncture.
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3986
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Third Party Eligible

No Linked CFR Text

Product code SBZ is linked to regulation 21CFR866.3986, which does not seem to exist yet. It may be pending at the moment.

Test For Detection Of Antibodies Associated With Syphilis Performed By Lay Users

Page Type
Product Code
Definition
Test for detection of antibodies associated with syphilis performed by lay users is an in vitro diagnostic device used for detection of antibodies in clinical specimens for use in home settings, or similar environments. The device is intended to aid in diagnosis of syphilis and intended for prescription use or over-the-counter use.
Physical State
Plastic cassette containing nitrocellulose membrane embedded with reagents capable of identifying analyte-specific antibodies in a blood sample.
Technical Method
Immobilization and visualization of antibodies specific to Syphilis disease using lateral flow technology.
Target Area
Blood drop exposed on the fingertip via fingerstick puncture.
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3986
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Third Party Eligible

No Linked CFR Text

Product code SBZ is linked to regulation 21CFR866.3986, which does not seem to exist yet. It may be pending at the moment.