Product code DPD— Clinical Toxicology
ELECTRONIC STETHOSCOPE
- Classification name
- Radioimmunoassay, Digoxin (3-H), Rabbit 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 DPD
FDA has cleared device under product code DPD, all in 1977, 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 DPD
Recent clearances under product code DPD
Data sourced from openFDA. This site is unofficial and independent of the FDA.