Product code JAO— Radiology
ABIOMED BODY LEAD ANALYZER MODEL 200/20
- Classification name
- Scanner, Fluorescent
- Device class
- Class 2
- Regulation
- 21 CFR 892.1220
- Advisory panel
- Radiology
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code JAO
FDA has cleared devices under product code JAO between 1990 and 1991, 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
- 1991
- 1990
Top applicants under product code JAO
Recent clearances under product code JAO
Data sourced from openFDA. This site is unofficial and independent of the FDA.