Product code HAD— Neurology
AESCULAP PNEUMATIC KERRISON
- Classification name
- Rongeur, Powered
- Device class
- Class 2
- Regulation
- 21 CFR 882.4845
- Advisory panel
- Neurology
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code HAD
FDA has cleared devices under product code HAD between 1991 and 2006, filed by 3 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
- 2006
- 2002
- 1991
Top applicants under product code HAD
Recent clearances under product code HAD
Data sourced from openFDA. This site is unofficial and independent of the FDA.