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FDA 510(k)

GELPORT BLUNT TIP TROCAR SYSTEM

K-Number: K060629 · 2006-04-07

ApplicantApplied Medical Resources Corp.
Decision Date2006-04-07
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GELPORT BLUNT TIP 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 2006-04-07 under 510(k) number K060629. 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 GELPORT BLUNT TIP TROCAR SYSTEM?

GELPORT BLUNT TIP TROCAR SYSTEM is a medical device that received FDA 510(k) clearance on 2006-04-07. The listed applicant is Applied Medical Resources Corp.. The 510(k) number is K060629.

When did GELPORT BLUNT TIP TROCAR SYSTEM receive FDA 510(k) clearance?

GELPORT BLUNT TIP TROCAR SYSTEM received FDA 510(k) clearance on 2006-04-07, under 510(k) number K060629.

Who is the listed applicant for GELPORT BLUNT TIP 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 GELPORT BLUNT TIP TROCAR SYSTEM?

The FDA product code for GELPORT BLUNT TIP TROCAR SYSTEM 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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