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FDA 510(k)

KII TROCAR SYSTEM

K-Number: K072674 · 2007-10-05

ApplicantApplied Medical Resources Corp.
Decision Date2007-10-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KII TROCAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources Corp.. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K072674. 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 KII TROCAR SYSTEM?

KII TROCAR SYSTEM is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is Applied Medical Resources Corp.. The 510(k) number is K072674.

When did KII TROCAR SYSTEM receive FDA 510(k) clearance?

KII TROCAR SYSTEM received FDA 510(k) clearance on 2007-10-05, under 510(k) number K072674.

Who is the listed applicant for KII TROCAR SYSTEM?

The FDA 510(k) record lists Applied Medical Resources Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KII TROCAR SYSTEM?

The FDA product code for KII TROCAR SYSTEM is GCJ.

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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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