SteriTite rigid reusable sterilization container with MediTray Products
K-Number: K240898 · 2024-07-31
Device Summary
Frequently Asked Questions
What is the SteriTite rigid reusable sterilization container with MediTray Products?
SteriTite rigid reusable sterilization container with MediTray Products is a medical device that received FDA 510(k) clearance on 2024-07-31. The listed applicant is Case Medical. The 510(k) number is K240898.
When did SteriTite rigid reusable sterilization container with MediTray Products receive FDA 510(k) clearance?
SteriTite rigid reusable sterilization container with MediTray Products received FDA 510(k) clearance on 2024-07-31, under 510(k) number K240898.
Who is the listed applicant for SteriTite rigid reusable sterilization container with MediTray Products?
The FDA 510(k) record lists Case Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SteriTite rigid reusable sterilization container with MediTray Products?
The FDA product code for SteriTite rigid reusable sterilization container with MediTray Products is KCT.
Other records listing Case Medical 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.