DeviceClearance

Product code DMR— Clinical Toxicology

RF CONTROLS

Classification name
Solution, M-Nitrophenol, Specific Reagent For Cholinesterase
Device class
Class 1
Regulation
21 CFR 862.3240
Advisory panel
Clinical Toxicology
Total cleared
1
First cleared
Most recent

Market context for product code DMR

FDA has cleared 1 device under product code DMR, all in 1979, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code DMR

Recent clearances under product code DMR

Data sourced from openFDA. This site is unofficial and independent of the FDA.