Culture Media, For Isolation Of Pathogenic Neisseria

Device Code: 3368

Product Code(s): JTY

Device Classification Information

Device Type ID3368
Device NameCulture Media, For Isolation Of Pathogenic Neisseria
Regulation DescriptionCulture Medium For Pathogenic Neisseria Spp.
Regulation Medical SpecialtyMicrobiology
Review PanelMicrobiology
Premarket Review Office Of In Vitro Diagnostics And Radiological Health (OIR)
Submission Type510(k)
CFR Regulation Number866.2410 [🔎]
FDA Device ClassificationClass 2 Medical Device
Product CodeJTY
GMP ExemptNo
Summary MREligible
Implanted DeviceNo
Life Support DeviceNo
Third Party Review Not Third Party Eligible

Recognized Standards

Total Product Life Cycle

Device Type ID3368
DeviceCulture Media, For Isolation Of Pathogenic Neisseria
Product CodeJTY
FDA Device ClassificationClass 2 Medical Device
Regulation DescriptionCulture Medium For Pathogenic Neisseria Spp.
CFR Regulation Number866.2410 [🔎]
Recalls
Manufacturer Recall Class Date Posted
1
Becton Dickinson & Co.
II Aug-17-2018
TPLC Last Update: 2019-04-02 20:28:19

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.