Intuitive Surgical Instrument and Accessories Sterilization Trays

FDA 510(k) K072211 · Intuitive Surgical, Inc.

Substantially Equivalent

510(k) numberK072211

Submission

Device name
Intuitive Surgical Instrument and Accessories Sterilization Trays
Applicant
Intuitive Surgical, Inc.
Sunnyvale, CA, US
Received
August 9, 2007
Decision date
February 28, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

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 Intuitive Surgical Instrument and Accessories Sterilization Trays cleared by the FDA?

Intuitive Surgical Instrument and Accessories Sterilization Trays (K072211) received a 510(k) decision of Substantially Equivalent on February 28, 2008, 203 days after the submission was received.

What is the product code of K072211?

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.