Codman Sterilization Containers

FDA 510(k) K092437 · Codman & Shurtleff, Inc.

Substantially Equivalent

510(k) numberK092437

Submission

Device name
Codman Sterilization Containers
Applicant
Codman & Shurtleff, Inc.
Raynham, MA, US
Received
August 7, 2009
Decision date
March 25, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KCT – Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6850
Specialty
General Hospital

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Questions and answers

When was Codman Sterilization Containers cleared by the FDA?

Codman Sterilization Containers (K092437) received a 510(k) decision of Substantially Equivalent on March 25, 2010, 230 days after the submission was received.

What is the product code of K092437?

The FDA product code is KCT – Sterilization Wrap Containers, Trays, Cassettes & Other Accessories, a Class II (moderate risk) device regulated under 21 CFR 880.6850.