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FDA 510(k)

TROCAR CANNULA STABILIZER

K-Number: K950005 · 1995-01-18

ApplicantAdvanced Surgical, Inc.
Decision Date1995-01-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TROCAR CANNULA STABILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Surgical, Inc.. It received FDA 510(k) clearance on 1995-01-18 under 510(k) number K950005. 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 TROCAR CANNULA STABILIZER?

TROCAR CANNULA STABILIZER is a medical device that received FDA 510(k) clearance on 1995-01-18. The listed applicant is Advanced Surgical, Inc.. The 510(k) number is K950005.

When did TROCAR CANNULA STABILIZER receive FDA 510(k) clearance?

TROCAR CANNULA STABILIZER received FDA 510(k) clearance on 1995-01-18, under 510(k) number K950005.

Who is the listed applicant for TROCAR CANNULA STABILIZER?

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

What is the FDA product code for TROCAR CANNULA STABILIZER?

The FDA product code for TROCAR CANNULA STABILIZER is GCJ.

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Other records listing Advanced Surgical, Inc. as applicant

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Related Devices (Code: GCJ)

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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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