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FDA 510(k)

MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE.

K-Number: K895841 · 1989-11-15

ApplicantEverest Medical Corp.
Decision Date1989-11-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE. 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 1989-11-15 under 510(k) number K895841. 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 MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE.?

MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE. is a medical device that received FDA 510(k) clearance on 1989-11-15. The listed applicant is Everest Medical Corp.. The 510(k) number is K895841.

When did MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE. receive FDA 510(k) clearance?

MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE. received FDA 510(k) clearance on 1989-11-15, under 510(k) number K895841.

Who is the listed applicant for MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE.?

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 MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE.?

The FDA product code for MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE. 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.

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