Product code DLR— Clinical Toxicology
HI-M-TEST MORPHINE
- Classification name
- Hemagglutination Inhibition, Morphine
- Device class
- Class 2
- Regulation
- 21 CFR 862.3640
- Advisory panel
- Clinical Toxicology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code DLR
FDA has cleared devices under product code DLR between 1976 and 1979, filed by 2 applicant companies. 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.
Clearances per year
- 1979
- 1976
Top applicants under product code DLR
Recent clearances under product code DLR
Data sourced from openFDA. This site is unofficial and independent of the FDA.