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FDA 510(k)

SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM

K-Number: K071571 · 2007-07-30

Decision Date2007-07-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Surgiquest, Inc.. It received FDA 510(k) clearance on 2007-07-30 under 510(k) number K071571. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM?

SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM is a medical device that received FDA 510(k) clearance on 2007-07-30. The listed applicant is Surgiquest, Inc.. The 510(k) number is K071571.

When did SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM receive FDA 510(k) clearance?

SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM received FDA 510(k) clearance on 2007-07-30, under 510(k) number K071571.

Who is the listed applicant for SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM?

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

What is the FDA product code for SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM?

The FDA product code for SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM is GCJ.

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 Surgiquest, 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 8 devices →

Related Devices (Code: GCJ)

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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