510(k) K023614

STERITITE RIGID REUSABLE STERILIZATION CONTAINER SYSTEM by Case Medical, Inc. — Product Code FRG

K023614 is an FDA 510(k) premarket notification submitted by Case Medical, Inc. for the device "STERITITE RIGID REUSABLE STERILIZATION CONTAINER SYSTEM". The FDA issued a decision of Substantially Equivalent on April 7, 2003. 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
April 7, 2003
Date Received
October 28, 2002
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