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FDA 510(k)

EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS

K-Number: K031081 · 2003-05-21

ApplicantGyrus Medical, Inc.
Decision Date2003-05-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Gyrus Medical, Inc.. It received FDA 510(k) clearance on 2003-05-21 under 510(k) number K031081. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS?

EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS is a medical device that received FDA 510(k) clearance on 2003-05-21. The listed applicant is Gyrus Medical, Inc.. The 510(k) number is K031081.

When did EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS receive FDA 510(k) clearance?

EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS received FDA 510(k) clearance on 2003-05-21, under 510(k) number K031081.

Who is the listed applicant for EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS?

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

What is the FDA product code for EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS?

The FDA product code for EVEREST LP BIPOLAR SCISSORS AND GYRUS LP BIPOLAR SCISSORS is GEI.

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Other records listing Gyrus Medical, Inc. as applicant

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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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