Product code DKG— Clinical Chemistry
EMIT D.A.U. LOW & MEDIUM CALIBRATOR A
- Classification name
- Plate, Cellulose, Tlc
- Device class
- Class 1
- Regulation
- 21 CFR 862.2270
- Advisory panel
- Clinical Chemistry
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code DKG
FDA has cleared device under product code DKG, all in 1989, 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 DKG
Recent clearances under product code DKG
Data sourced from openFDA. This site is unofficial and independent of the FDA.