Product code DOR— Clinical Toxicology

PERICARDIOCENTESIS KIT

Classification name
Radioimmunoassay, Digoxin (3-H), Bovine Antibody, Charcoal Sep.
Device class
Class 2
Regulation
21 CFR 862.3320
Advisory panel
Clinical Toxicology
Total cleared
1
First cleared
Most recent

Market context for product code DOR

FDA has cleared 1 device under product code DOR, all in 1980, 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 DOR

Recent clearances under product code DOR

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