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FDA 510(k)

EVERSHEARS BIPOLAR SCISSORS

K-Number: K000496 · 2000-04-24

ApplicantEverest Medical Corp.
Decision Date2000-04-24
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EVERSHEARS BIPOLAR SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Everest Medical Corp.. It received FDA 510(k) clearance on 2000-04-24 under 510(k) number K000496. 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 EVERSHEARS BIPOLAR SCISSORS?

EVERSHEARS BIPOLAR SCISSORS is a medical device that received FDA 510(k) clearance on 2000-04-24. The listed applicant is Everest Medical Corp.. The 510(k) number is K000496.

When did EVERSHEARS BIPOLAR SCISSORS receive FDA 510(k) clearance?

EVERSHEARS BIPOLAR SCISSORS received FDA 510(k) clearance on 2000-04-24, under 510(k) number K000496.

Who is the listed applicant for EVERSHEARS BIPOLAR SCISSORS?

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

What is the FDA product code for EVERSHEARS BIPOLAR SCISSORS?

The FDA product code for EVERSHEARS BIPOLAR SCISSORS is GEI.

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Other records listing Everest 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.

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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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