510(k) K112904

STERITEC CONTAINERS SYSTEM & MEDITRAY PRODUCTS by Case Medical, Inc. — Product Code FRG

K112904 is an FDA 510(k) premarket notification submitted by Case Medical, Inc. for the device "STERITEC CONTAINERS SYSTEM & MEDITRAY PRODUCTS". The FDA issued a decision of Substantially Equivalent on January 24, 2012. The device falls under product code FRG (Wrap, Sterilization), a Class II device regulated under 21 CFR 880.6850. Case Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 2012
Date Received
October 4, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Wrap, Sterilization
Device Class
Class II
Regulation Number
880.6850
Review Panel
HO
Submission Type