DeviceClearance

Product code ILQ— Physical Medicine

ALARM INTERCOM DOOR LOCK

Classification name
System, Communication, Powered
Device class
Class 2
Regulation
21 CFR 890.3710
Advisory panel
Physical Medicine
Total cleared
38
First cleared
Most recent

Market context for product code ILQ

FDA has cleared 38 devices under product code ILQ between 1977 and 2017, filed by 26 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 ILQ

Adverse events under product code ILQ

product code ILQ
Death
4
Malfunction
477
Total
481

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 ILQ

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