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FDA 510(k)

Endoscope Sterilization Tray

K-Number: K170640 · 2017-09-17

Decision Date2017-09-17
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Endoscope Sterilization Tray 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 2017-09-17 under 510(k) number K170640. 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 Endoscope Sterilization Tray?

Endoscope Sterilization Tray is a medical device that received FDA 510(k) clearance on 2017-09-17. The listed applicant is Intuitive Surgical, Inc.. The 510(k) number is K170640.

When did Endoscope Sterilization Tray receive FDA 510(k) clearance?

Endoscope Sterilization Tray received FDA 510(k) clearance on 2017-09-17, under 510(k) number K170640.

Who is the listed applicant for Endoscope Sterilization Tray?

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 Endoscope Sterilization Tray?

The FDA product code for Endoscope Sterilization Tray 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.

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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.