DeviceClearance

PRO-LITE Sterilization Tray— 510(k) K231501

Substantially Equivalent

STERIS Corporation

FDA 510(k) clearance K231501 for PRO-LITE Sterilization Tray, Substantially Equivalent on 2023-08-07. Applicant: STERIS Corporation.

Clearance details

Applicant
STERIS Corporation
Product code
Code KCT
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mentor, OH, US
Download summary PDFView on FDA.gov ↗

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