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FDA 510(k)

TROGARD TROCAR DIALATING TROCAR SYSTEM

K-Number: K961175 · 1996-04-05

ApplicantConmedcorp
Decision Date1996-04-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TROGARD TROCAR DIALATING TROCAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1996-04-05 under 510(k) number K961175. 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 TROGARD TROCAR DIALATING TROCAR SYSTEM?

TROGARD TROCAR DIALATING TROCAR SYSTEM is a medical device that received FDA 510(k) clearance on 1996-04-05. The listed applicant is Conmedcorp. The 510(k) number is K961175.

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

TROGARD TROCAR DIALATING TROCAR SYSTEM received FDA 510(k) clearance on 1996-04-05, under 510(k) number K961175.

Who is the listed applicant for TROGARD TROCAR DIALATING TROCAR SYSTEM?

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

What is the FDA product code for TROGARD TROCAR DIALATING TROCAR SYSTEM?

The FDA product code for TROGARD TROCAR DIALATING TROCAR SYSTEM is GCJ.

Related Clinical Trials

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.

Other records listing Conmedcorp as applicant

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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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.

Official Source

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

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