Product code MDZ— General Hospital
DECOMAT 228
- Classification name
- Cleaners, Medical Devices
- Device class
- Class 2
- Regulation
- 21 CFR 880.6992
- Advisory panel
- General Hospital
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code MDZ
FDA has cleared devices under product code MDZ, all in 1994, 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 MDZ
Recent clearances under product code MDZ
Data sourced from openFDA. This site is unofficial and independent of the FDA.