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FDA 510(k)

INTUITIVE SURGICAL INSTRUMENT AND ACCESSORIES STERILIZATION TRAYS

K-Number: K072211 · 2008-02-28

Decision Date2008-02-28
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTUITIVE SURGICAL INSTRUMENT AND ACCESSORIES STERILIZATION TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2008-02-28 under 510(k) number K072211. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTUITIVE SURGICAL INSTRUMENT AND ACCESSORIES STERILIZATION TRAYS?

INTUITIVE SURGICAL INSTRUMENT AND ACCESSORIES STERILIZATION TRAYS is a medical device that received FDA 510(k) clearance on 2008-02-28. The listed applicant is Intuitive Surgical, Inc.. The 510(k) number is K072211.

When did INTUITIVE SURGICAL INSTRUMENT AND ACCESSORIES STERILIZATION TRAYS receive FDA 510(k) clearance?

INTUITIVE SURGICAL INSTRUMENT AND ACCESSORIES STERILIZATION TRAYS received FDA 510(k) clearance on 2008-02-28, under 510(k) number K072211.

Who is the listed applicant for INTUITIVE SURGICAL INSTRUMENT AND ACCESSORIES STERILIZATION TRAYS?

The FDA 510(k) record lists Intuitive Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTUITIVE SURGICAL INSTRUMENT AND ACCESSORIES STERILIZATION TRAYS?

The FDA product code for INTUITIVE SURGICAL INSTRUMENT AND ACCESSORIES STERILIZATION TRAYS is KCT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Intuitive Surgical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 164 devices →

Related Devices (Code: KCT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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