FDA 510(k)

EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS

K-Number: K945975 · 1994-12-21

Decision Date1994-12-21

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS 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 1994-12-21 under 510(k) number K945975. 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(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS?

EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS is a medical device that received FDA 510(k) clearance on 1994-12-21. The listed applicant is Everest Medical Corp.. The 510(k) number is K945975.

When did EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS receive FDA 510(k) clearance?

EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS received FDA 510(k) clearance on 1994-12-21, under 510(k) number K945975.

Who is the listed applicant for EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS?

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(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS?

The FDA product code for EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS is GEI.

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Other records listing Everest Medical Corp. 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.