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FDA 510(k)

ENDO-GARD ELECTROSURGICAL TROCAR

K-Number: K915790 · 1992-10-09

ApplicantConmedcorp
Decision Date1992-10-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDO-GARD ELECTROSURGICAL TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1992-10-09 under 510(k) number K915790. 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 ENDO-GARD ELECTROSURGICAL TROCAR?

ENDO-GARD ELECTROSURGICAL TROCAR is a medical device that received FDA 510(k) clearance on 1992-10-09. The listed applicant is Conmedcorp. The 510(k) number is K915790.

When did ENDO-GARD ELECTROSURGICAL TROCAR receive FDA 510(k) clearance?

ENDO-GARD ELECTROSURGICAL TROCAR received FDA 510(k) clearance on 1992-10-09, under 510(k) number K915790.

Who is the listed applicant for ENDO-GARD ELECTROSURGICAL TROCAR?

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 ENDO-GARD ELECTROSURGICAL TROCAR?

The FDA product code for ENDO-GARD ELECTROSURGICAL 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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