Product code DOK— Clinical Toxicology

RUBELLA LATEX CARD TEST

Classification name
Free Radical Assay, Morphine
Device class
Class 2
Regulation
21 CFR 862.3640
Advisory panel
Clinical Toxicology
Total cleared
1
First cleared
Most recent

Market context for product code DOK

FDA has cleared 1 device under product code DOK, all in 1981, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Top applicants under product code DOK

Recent clearances under product code DOK

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