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FDA 510(k)

SURGICAL TROCAR

K-Number: K911462 · 1991-04-22

ApplicantApplied Medical
Decision Date1991-04-22
Product CodeDRC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SURGICAL TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical. It received FDA 510(k) clearance on 1991-04-22 under 510(k) number K911462. 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 SURGICAL TROCAR?

SURGICAL TROCAR is a medical device that received FDA 510(k) clearance on 1991-04-22. The listed applicant is Applied Medical. The 510(k) number is K911462.

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

SURGICAL TROCAR received FDA 510(k) clearance on 1991-04-22, under 510(k) number K911462.

Who is the listed applicant for SURGICAL TROCAR?

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

What is the FDA product code for SURGICAL TROCAR?

The FDA product code for SURGICAL TROCAR is DRC.

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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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