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FDA 510(k)

FUNNEL TROCAR

K-Number: K992324 · 1999-08-19

Decision Date1999-08-19
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FUNNEL TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Patton Medical Corp.. It received FDA 510(k) clearance on 1999-08-19 under 510(k) number K992324. 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 FUNNEL TROCAR?

FUNNEL TROCAR is a medical device that received FDA 510(k) clearance on 1999-08-19. The listed applicant is Patton Medical Corp.. The 510(k) number is K992324.

When did FUNNEL TROCAR receive FDA 510(k) clearance?

FUNNEL TROCAR received FDA 510(k) clearance on 1999-08-19, under 510(k) number K992324.

Who is the listed applicant for FUNNEL TROCAR?

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

What is the FDA product code for FUNNEL TROCAR?

The FDA product code for FUNNEL TROCAR 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 Patton Medical Corp. 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.

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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