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FDA 510(k)

LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA

K-Number: K922509 · 1992-10-01

ApplicantEverest Medical Corp.
Decision Date1992-10-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA 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 1992-10-01 under 510(k) number K922509. 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 LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA?

LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA is a medical device that received FDA 510(k) clearance on 1992-10-01. The listed applicant is Everest Medical Corp.. The 510(k) number is K922509.

When did LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA receive FDA 510(k) clearance?

LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA received FDA 510(k) clearance on 1992-10-01, under 510(k) number K922509.

Who is the listed applicant for LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA?

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 LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA?

The FDA product code for LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA is GEI.

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Other records listing Everest Medical Corp. as applicant

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Related Devices (Code: GEI)

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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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