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FDA 510(k)

BASX BLADELESS TROCAR

K-Number: K062209 · 2006-10-10

ApplicantEthicon Endo-Surgery, LLC
Decision Date2006-10-10
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BASX BLADELESS TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, LLC. It received FDA 510(k) clearance on 2006-10-10 under 510(k) number K062209. 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 BASX BLADELESS TROCAR?

BASX BLADELESS TROCAR is a medical device that received FDA 510(k) clearance on 2006-10-10. The listed applicant is Ethicon Endo-Surgery, LLC. The 510(k) number is K062209.

When did BASX BLADELESS TROCAR receive FDA 510(k) clearance?

BASX BLADELESS TROCAR received FDA 510(k) clearance on 2006-10-10, under 510(k) number K062209.

Who is the listed applicant for BASX BLADELESS TROCAR?

The FDA 510(k) record lists Ethicon Endo-Surgery, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BASX BLADELESS TROCAR?

The FDA product code for BASX BLADELESS TROCAR is 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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