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FDA 510(k)

INTUITIVE SURGICAL ULTRASONIC SHEARS

K-Number: K011281 · 2001-07-24

Decision Date2001-07-24
Product CodeNAY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INTUITIVE SURGICAL ULTRASONIC SHEARS 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 2001-07-24 under 510(k) number K011281. The device is classified under product code NAY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTUITIVE SURGICAL ULTRASONIC SHEARS?

INTUITIVE SURGICAL ULTRASONIC SHEARS is a medical device that received FDA 510(k) clearance on 2001-07-24. The listed applicant is Intuitive Surgical, Inc.. The 510(k) number is K011281.

When did INTUITIVE SURGICAL ULTRASONIC SHEARS receive FDA 510(k) clearance?

INTUITIVE SURGICAL ULTRASONIC SHEARS received FDA 510(k) clearance on 2001-07-24, under 510(k) number K011281.

Who is the listed applicant for INTUITIVE SURGICAL ULTRASONIC SHEARS?

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 ULTRASONIC SHEARS?

The FDA product code for INTUITIVE SURGICAL ULTRASONIC SHEARS is NAY.

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: NAY)

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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