DeviceClearance

Product code KCT— General Hospital

Endoscope Sterilization Tray

Classification name
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device class
Class 2
Regulation
21 CFR 880.6850
Advisory panel
General Hospital
Total cleared
282
First cleared
Most recent

Market context for product code KCT

FDA has cleared 282 devices under product code KCT between 1976 and 2026, filed by 156 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 KCT

Recent clearances under product code KCT

1–100 of 282

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