SteriTite Container System with MediTray Products
K-Number: K252854 · 2026-06-03
Device Summary
Frequently Asked Questions
What is the SteriTite Container System with MediTray Products?
SteriTite Container System with MediTray Products is a medical device that received FDA 510(k) clearance on 2026-06-03. The listed applicant is Case Medical, Inc.. The 510(k) number is K252854.
When did SteriTite Container System with MediTray Products receive FDA 510(k) clearance?
SteriTite Container System with MediTray Products received FDA 510(k) clearance on 2026-06-03, under 510(k) number K252854.
Who is the listed applicant for SteriTite Container System with MediTray Products?
The FDA 510(k) record lists Case Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SteriTite Container System with MediTray Products?
The FDA product code for SteriTite Container System with MediTray Products is KCT.
Other records listing Case Medical, Inc. 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.