U.v. Spectrometry, Tricyclic Antidepressant Drugs

Device Code: 6219

Product Code(s): LFH

Device Classification Information

Device Type ID6219
Device NameU.v. Spectrometry, Tricyclic Antidepressant Drugs
Regulation DescriptionTricyclic Antidepressant Drugs Test System.
Regulation Medical SpecialtyToxicology
Review PanelToxicology
Premarket Review Office Of In Vitro Diagnostics And Radiological Health (OIR)
Submission Type510(k)
CFR Regulation Number862.3910 [🔎]
FDA Device ClassificationClass 2 Medical Device
Product CodeLFH
GMP ExemptNo
Summary MREligible
Implanted DeviceNo
Life Support DeviceNo
Third Party Review Eligible For Accredited Persons Expansion Pilot Program

Recognized Standards

Total Product Life Cycle

Device Type ID6219
DeviceU.v. Spectrometry, Tricyclic Antidepressant Drugs
Product CodeLFH
FDA Device ClassificationClass 2 Medical Device
Regulation DescriptionTricyclic Antidepressant Drugs Test System.
CFR Regulation Number862.3910 [🔎]
Recalls
Manufacturer Recall Class Date Posted
1
Ameditech Inc
III Apr-28-2018
2
Ameditech Inc
III Aug-29-2017
TPLC Last Update: 2019-04-02 21:18:57

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