Sterilization Tray
K-Number: K160912 · 2016-10-07
Device Summary
Frequently Asked Questions
What is the Sterilization Tray?
Sterilization Tray is a medical device that received FDA 510(k) clearance on 2016-10-07. The listed applicant is STERIS Corporation. The 510(k) number is K160912.
When did Sterilization Tray receive FDA 510(k) clearance?
Sterilization Tray received FDA 510(k) clearance on 2016-10-07, under 510(k) number K160912.
Who is the listed applicant for Sterilization Tray?
The FDA 510(k) record lists STERIS Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sterilization Tray?
The FDA product code for Sterilization Tray is KCT.
Other records listing STERIS Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KCT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.