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FDA 510(k)

SURGIQUEST ANCHORPORT SIL KIT

K-Number: K100180 · 2010-05-05

ApplicantSurgiquest, Inc.
Decision Date2010-05-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SURGIQUEST ANCHORPORT SIL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Surgiquest, Inc.. It received FDA 510(k) clearance on 2010-05-05 under 510(k) number K100180. 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 ANCHORPORT SIL KIT?

SURGIQUEST ANCHORPORT SIL KIT is a medical device that received FDA 510(k) clearance on 2010-05-05. The listed applicant is Surgiquest, Inc.. The 510(k) number is K100180.

When did SURGIQUEST ANCHORPORT SIL KIT receive FDA 510(k) clearance?

SURGIQUEST ANCHORPORT SIL KIT received FDA 510(k) clearance on 2010-05-05, under 510(k) number K100180.

Who is the listed applicant for SURGIQUEST ANCHORPORT SIL KIT?

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 ANCHORPORT SIL KIT?

The FDA product code for SURGIQUEST ANCHORPORT SIL KIT is GCJ.

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Other records listing Surgiquest, Inc. as applicant

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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.

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Official Source

View on FDA Database →

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

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