Product code KPD— General Hospital

FEVER TESTER

Classification name
Strip, Temperature, Forehead, Liquid Crystal
Device class
Class 2
Regulation
21 CFR 880.2200
Advisory panel
General Hospital
Total cleared
21
First cleared
Most recent

Market context for product code KPD

FDA has cleared 21 devices under product code KPD between 1976 and 1994, filed by 18 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 KPD

Recent clearances under product code KPD

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