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FDA 510(k)

ENDOSURG DISPOSABLE SECONDARY TROCAR

K-Number: K940036 · 1994-05-12

ApplicantEndosurg
Decision Date1994-05-12
Product CodeDRC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ENDOSURG DISPOSABLE SECONDARY TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Endosurg. It received FDA 510(k) clearance on 1994-05-12 under 510(k) number K940036. The device is classified under product code DRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSURG DISPOSABLE SECONDARY TROCAR?

ENDOSURG DISPOSABLE SECONDARY TROCAR is a medical device that received FDA 510(k) clearance on 1994-05-12. The listed applicant is Endosurg. The 510(k) number is K940036.

When did ENDOSURG DISPOSABLE SECONDARY TROCAR receive FDA 510(k) clearance?

ENDOSURG DISPOSABLE SECONDARY TROCAR received FDA 510(k) clearance on 1994-05-12, under 510(k) number K940036.

Who is the listed applicant for ENDOSURG DISPOSABLE SECONDARY TROCAR?

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

What is the FDA product code for ENDOSURG DISPOSABLE SECONDARY TROCAR?

The FDA product code for ENDOSURG DISPOSABLE SECONDARY TROCAR is DRC.

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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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