DeviceClearance

Product code JCX— General, Plastic Surgery

CLIQ DV-300 ASPIRATOR

Classification name
Apparatus, Suction, Ward Use, Portable, Ac-Powered
Device class
Class 2
Regulation
21 CFR 878.4780
Advisory panel
General, Plastic Surgery
Total cleared
77
First cleared
Most recent

Market context for product code JCX

FDA has cleared 77 devices under product code JCX between 1977 and 2026, filed by 52 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

last 15 years

Top applicants under product code JCX

Adverse events under product code JCX

product code JCX
Death
11
Malfunction
838
Other
1
Total
850

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code JCX

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