FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SteriTite Container System with MediTray Products

K Number: K252854 · Decision Jun 3, 2026
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
15
Review Days
268

Basic Information

Device Name
SteriTite Container System with MediTray Products
K Number
K252854
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Case Medical, Inc.
Date Received
September 8, 2025
Decision Date
June 3, 2026
Product Code
KCT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

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K Number Device Name
K221492 SteriTite Container System with MediTray Parts
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K161415 SteriTite Containers System & MediTray Products
K112904 STERITEC CONTAINERS SYSTEM & MEDITRAY PRODUCTS
K110682 STERITITE CONTAINER SYSTEM & MEDITRAY PRODUCTS
K090068 STERITITE UNIVERSAL CONTAINER SYSTEM AND MEDITRAY PRODUCTS
K080558 STERITITE CONTAINER SYSTEM & MEDITRAY PRODUCTS
K022978 STERITITE CONTAINER WITH FLASHTITE VALVE PLATE(S) & MEDITRAY PRODUCTS
K023614 STERITITE RIGID REUSABLE STERILIZATION CONTAINER SYSTEM
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