Product code HCI— Neurology

Aesculap Slim Clip Applier

Classification name
Applier, Aneurysm Clip
Device class
Class 2
Regulation
21 CFR 882.4175
Advisory panel
Neurology
Total cleared
14
First cleared
Most recent

Market context for product code HCI

FDA has cleared 14 devices under product code HCI between 1983 and 2022, filed by 9 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

Top applicants under product code HCI

Recent clearances under product code HCI

Data sourced from openFDA. This site is unofficial and independent of the FDA.