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FDA 510(k)

SteriTite Container System with MediTray Products

K-Number: K252854 · 2026-06-03

Decision Date2026-06-03
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SteriTite Container System with MediTray Products is the device name listed in this FDA 510(k) record. The listed applicant is Case Medical, Inc.. It received FDA 510(k) clearance on 2026-06-03 under 510(k) number K252854. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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